Canonical Allele Identifier: CA490206539

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711196-T-A
• MyVariant Identifiers: chr15:g.45003394T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711196T>A , CM000677.2:g.44711196T>A	GRCh38
NC_000015.9:g.45003394T>A , CM000677.1:g.45003394T>A	GRCh37
NC_000015.8:g.42790686T>A	NCBI36
NG_012920.1:g.4710T>A
NG_012920.2:g.4720T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-430A>T MANE Select	ENSP00000508024.1:n.-430A>T
ENST00000558573.1:n.121A>T
XM_011521338.1:c.-430A>T	XP_011519640.1:n.-430A>T
XM_011521339.1:c.-311A>T	XP_011519641.1:n.-311A>T
XM_011521340.1:c.-252A>T	XP_011519642.1:n.-252A>T
XM_011521343.1:c.-514A>T	XP_011519645.1:n.-514A>T
XM_011521345.1:c.-485A>T	XP_011519647.1:n.-485A>T
XM_011521338.3:c.-430A>T	XP_011519640.1:n.-430A>T
XM_011521339.3:c.-311A>T	XP_011519641.1:n.-311A>T
XM_011521340.3:c.-252A>T	XP_011519642.1:n.-252A>T
XM_011521343.3:c.-514A>T	XP_011519645.1:n.-514A>T
XM_011521345.3:c.-485A>T	XP_011519647.1:n.-485A>T
NM_001387260.1:c.-76+136A>T	NP_001374189.1:n.-76+136A>T
NM_001387261.1:c.-252A>T	NP_001374190.1:n.-252A>T
NM_001387262.1:c.-520A>T	NP_001374191.1:n.-520A>T
NM_001387263.1:c.-430A>T MANE Select	NP_001374192.1:n.-430A>T