Canonical Allele Identifier: CA382171724

Gene: PAK1

Linked Data

• gnomAD v4: 11-77392477-G-A
• MyVariant Identifiers: chr11:g.77103522G>A (hg19) ; chr11:g.77392477G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77392477G>A , CM000673.2:g.77392477G>A	GRCh38
NC_000011.9:g.77103522G>A , CM000673.1:g.77103522G>A	GRCh37
NC_000011.8:g.76781170G>A	NCBI36
NG_029900.1:g.86587C>T
NG_029900.2:g.86587C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356341.8:c.44C>T MANE Select	ENSP00000348696.4:p.Pro15Leu
ENST00000278568.8:c.44C>T	ENSP00000278568.4:p.Pro15Leu
ENST00000356341.7:c.44C>T	ENSP00000348696.3:p.Pro15Leu
ENST00000524847.5:c.44C>T	ENSP00000432477.1:p.Pro15Leu
ENST00000526968.1:c.44C>T	ENSP00000433737.1:p.Pro15Leu
ENST00000528203.5:c.-104-12483C>T	ENSP00000433211.1:n.-104-12483C>T
ENST00000528592.5:c.44C>T	ENSP00000433004.1:p.Pro15Leu
ENST00000528633.1:c.44C>T	ENSP00000435983.1:p.Pro15Leu
ENST00000529248.5:c.44C>T	ENSP00000433518.1:p.Pro15Leu
ENST00000530617.5:c.44C>T	ENSP00000433423.1:p.Pro15Leu
ENST00000533568.5:n.152C>T
NM_001128620.1:c.44C>T	NP_001122092.1:p.Pro15Leu
NM_002576.4:c.44C>T	NP_002567.3:p.Pro15Leu
XM_011545080.1:c.44C>T	XP_011543382.1:p.Pro15Leu
XM_011545081.1:c.44C>T	XP_011543383.1:p.Pro15Leu
XM_011545082.1:c.44C>T	XP_011543384.1:p.Pro15Leu
XM_011545083.1:c.44C>T	XP_011543385.1:p.Pro15Leu
XM_011545084.1:c.44C>T	XP_011543386.1:p.Pro15Leu
XM_011545080.3:c.44C>T	XP_011543382.1:p.Pro15Leu
XM_011545081.2:c.44C>T	XP_011543383.1:p.Pro15Leu
XM_011545082.2:c.44C>T	XP_011543384.1:p.Pro15Leu
XM_011545083.2:c.44C>T	XP_011543385.1:p.Pro15Leu
XM_011545084.3:c.44C>T	XP_011543386.1:p.Pro15Leu
XM_017017846.1:c.44C>T	XP_016873335.1:p.Pro15Leu
XM_017017847.2:c.44C>T	XP_016873336.1:p.Pro15Leu
XM_017017848.1:c.44C>T	XP_016873337.1:p.Pro15Leu
XM_017017849.1:c.44C>T	XP_016873338.1:p.Pro15Leu
XM_017017850.1:c.44C>T	XP_016873339.1:p.Pro15Leu
XM_024448557.1:c.44C>T	XP_024304325.1:p.Pro15Leu
XM_024448558.1:c.44C>T	XP_024304326.1:p.Pro15Leu
XM_024448559.1:c.44C>T	XP_024304327.1:p.Pro15Leu
XM_024448560.1:c.44C>T	XP_024304328.1:p.Pro15Leu
XM_024448561.1:c.44C>T	XP_024304329.1:p.Pro15Leu
XM_024448562.1:c.44C>T	XP_024304330.1:p.Pro15Leu
XM_024448563.1:c.44C>T	XP_024304331.1:p.Pro15Leu
XM_024448564.1:c.44C>T	XP_024304332.1:p.Pro15Leu
NM_001128620.2:c.44C>T	NP_001122092.1:p.Pro15Leu
NM_001376268.1:c.44C>T	NP_001363197.1:p.Pro15Leu
NM_001376269.1:c.44C>T	NP_001363198.1:p.Pro15Leu
NM_001376270.1:c.44C>T	NP_001363199.1:p.Pro15Leu
NM_001376271.1:c.44C>T	NP_001363200.1:p.Pro15Leu
NM_001376272.1:c.44C>T	NP_001363201.1:p.Pro15Leu
NM_001376273.1:c.44C>T	NP_001363202.1:p.Pro15Leu
NM_001376274.1:c.44C>T	NP_001363203.1:p.Pro15Leu
NM_001376275.1:c.44C>T	NP_001363204.1:p.Pro15Leu
NM_001376276.1:c.44C>T	NP_001363205.1:p.Pro15Leu
NM_001376277.1:c.44C>T	NP_001363206.1:p.Pro15Leu
NM_001376278.1:c.44C>T	NP_001363207.1:p.Pro15Leu
NM_001376279.1:c.44C>T	NP_001363208.1:p.Pro15Leu
NM_001376280.1:c.44C>T	NP_001363209.1:p.Pro15Leu
NM_001376281.1:c.44C>T	NP_001363210.1:p.Pro15Leu
NM_001376282.1:c.44C>T	NP_001363211.1:p.Pro15Leu
NM_001376283.1:c.44C>T	NP_001363212.1:p.Pro15Leu
NM_001376284.1:c.44C>T	NP_001363213.1:p.Pro15Leu
NM_001376285.1:c.44C>T	NP_001363214.1:p.Pro15Leu
NM_001376286.1:c.44C>T	NP_001363215.1:p.Pro15Leu
NM_001376287.1:c.44C>T	NP_001363216.1:p.Pro15Leu
NM_001376288.1:c.44C>T	NP_001363217.1:p.Pro15Leu
NM_001376289.1:c.44C>T	NP_001363218.1:p.Pro15Leu
NM_001376290.1:c.44C>T	NP_001363219.1:p.Pro15Leu
NM_001376291.1:c.44C>T	NP_001363220.1:p.Pro15Leu
NM_001376292.1:c.44C>T	NP_001363221.1:p.Pro15Leu
NM_001376293.1:c.44C>T	NP_001363222.1:p.Pro15Leu
NM_001376294.1:c.44C>T	NP_001363223.1:p.Pro15Leu
NM_001376295.1:c.44C>T	NP_001363224.1:p.Pro15Leu
NM_001376301.1:c.44C>T	NP_001363230.1:p.Pro15Leu
NM_001376302.1:c.-104-12483C>T	NP_001363231.1:n.-104-12483C>T
NM_001376303.1:c.44C>T	NP_001363232.1:p.Pro15Leu
NM_001376304.1:c.-3-13089C>T	NP_001363233.1:n.-3-13089C>T
NM_001376305.1:c.-104-12483C>T	NP_001363234.1:n.-104-12483C>T
NM_002576.5:c.44C>T MANE Select	NP_002567.3:p.Pro15Leu
NR_164797.1:n.260C>T
NR_164798.1:n.263C>T