Canonical Allele Identifier: CA491335951

Gene: PSTPIP1

Linked Data

• gnomAD v4: 15-77032360-C-T
• MyVariant Identifiers: chr15:g.77324701C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77032360C>T , CM000677.2:g.77032360C>T	GRCh38
NC_000015.9:g.77324701C>T , CM000677.1:g.77324701C>T	GRCh37
NC_000015.8:g.75111756C>T	NCBI36
NG_007526.1:g.42237C>T , LRG_172:g.42237C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000697622.1:n.1503C>T
ENST00000697623.1:n.2223C>T
ENST00000558012.6:c.804C>T MANE Select	ENSP00000452746.1:p.Phe268=
ENST00000379595.7:c.804C>T	ENSP00000368914.3:p.Phe268=
ENST00000557995.1:n.468C>T
ENST00000558012.5:c.804C>T	ENSP00000452746.1:p.Phe268=
ENST00000558870.1:c.44C>T
ENST00000559295.5:c.804C>T	ENSP00000452743.1:p.Phe268=
ENST00000559785.5:c.999C>T	ENSP00000452986.1:p.Phe333=
ENST00000559856.1:c.723C>T	ENSP00000453382.1:p.Phe241=
ENST00000560223.5:c.*906C>T	ENSP00000454118.1:n.*906C>T
ENST00000560377.5:n.1045C>T
NM_003978.3:c.804C>T , LRG_172t1:c.804C>T	NP_003969.2:p.Phe268=
XM_006720737.2:c.438C>T	XP_006720800.1:p.Phe146=
XM_011522163.1:c.861C>T	XP_011520465.1:p.Phe287=
XM_011522164.1:c.759C>T	XP_011520466.1:p.Phe253=
XM_011522165.1:c.657C>T	XP_011520467.1:p.Phe219=
XM_011522166.1:c.861C>T	XP_011520468.1:p.Phe287=
XM_011522167.1:c.861C>T	XP_011520469.1:p.Phe287=
XM_011522168.1:c.861C>T	XP_011520470.1:p.Phe287=
XM_011522169.1:c.798+1082C>T	XP_011520471.1:n.798+1082C>T
XM_011522170.1:c.371+2786C>T	XP_011520472.1:n.371+2786C>T
XM_011522171.1:c.311+2786C>T	XP_011520473.1:n.311+2786C>T
XM_011522172.1:c.311+2786C>T	XP_011520474.1:n.311+2786C>T
XM_011522173.1:c.311+2786C>T	XP_011520475.1:n.311+2786C>T
XR_931936.1:n.1311C>T
XR_931937.1:n.1254C>T
XR_931938.1:n.1311C>T
XR_931939.1:n.1248+1082C>T
XR_931940.1:n.1069+2786C>T
NM_001321135.1:c.804C>T	NP_001308064.1:p.Phe268=
NM_001321136.1:c.777C>T	NP_001308065.1:p.Phe259=
NM_001321137.1:c.999C>T	NP_001308066.1:p.Phe333=
NM_003978.4:c.804C>T	NP_003969.2:p.Phe268=
NR_135552.1:n.1150+1082C>T
XM_006720737.3:c.438C>T	XP_006720800.1:p.Phe146=
XM_011522163.2:c.861C>T	XP_011520465.1:p.Phe287=
XM_011522165.2:c.657C>T	XP_011520467.1:p.Phe219=
XM_011522166.2:c.861C>T	XP_011520468.1:p.Phe287=
XM_011522167.2:c.861C>T	XP_011520469.1:p.Phe287=
XM_011522168.3:c.861C>T	XP_011520470.1:p.Phe287=
XM_011522169.2:c.798+1082C>T	XP_011520471.1:n.798+1082C>T
XR_931936.2:n.1309C>T
XR_931937.2:n.1252C>T
XR_931938.2:n.1309C>T
XR_931939.2:n.1246+1082C>T
NM_001321135.2:c.804C>T	NP_001308064.1:p.Phe268=
NM_001321136.2:c.777C>T	NP_001308065.1:p.Phe259=
NM_003978.5:c.804C>T MANE Select	NP_003969.2:p.Phe268=
NR_135552.2:n.1109+1082C>T