Canonical Allele Identifier: CA490206158

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711088-A-G
• MyVariant Identifiers: chr15:g.45003286A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711088A>G , CM000677.2:g.44711088A>G	GRCh38
NC_000015.9:g.45003286A>G , CM000677.1:g.45003286A>G	GRCh37
NC_000015.8:g.42790578A>G	NCBI36
NG_012920.1:g.4602A>G
NG_012920.2:g.4612A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-322T>C MANE Select	ENSP00000508024.1:n.-322T>C
ENST00000558573.1:n.229T>C
XM_011521338.1:c.-322T>C	XP_011519640.1:n.-322T>C
XM_011521339.1:c.-203T>C	XP_011519641.1:n.-203T>C
XM_011521340.1:c.-144T>C	XP_011519642.1:n.-144T>C
XM_011521343.1:c.-406T>C	XP_011519645.1:n.-406T>C
XM_011521345.1:c.-377T>C	XP_011519647.1:n.-377T>C
XM_011521338.3:c.-322T>C	XP_011519640.1:n.-322T>C
XM_011521339.3:c.-203T>C	XP_011519641.1:n.-203T>C
XM_011521340.3:c.-144T>C	XP_011519642.1:n.-144T>C
XM_011521343.3:c.-406T>C	XP_011519645.1:n.-406T>C
XM_011521345.3:c.-377T>C	XP_011519647.1:n.-377T>C
NM_001387260.1:c.-76+244T>C	NP_001374189.1:n.-76+244T>C
NM_001387261.1:c.-144T>C	NP_001374190.1:n.-144T>C
NM_001387262.1:c.-412T>C	NP_001374191.1:n.-412T>C
NM_001387263.1:c.-322T>C MANE Select	NP_001374192.1:n.-322T>C