Canonical Allele Identifier: CA2628214317

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711354-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711354A>T , CM000677.2:g.44711354A>T	GRCh38
NC_000015.9:g.45003552A>T , CM000677.1:g.45003552A>T	GRCh37
NC_000015.8:g.42790844A>T	NCBI36
NG_012920.1:g.4868A>T
NG_012920.2:g.4878A>T

Transcript Alleles

HGVS	Amino-acid Change
XM_011521338.1:c.-588T>A	XP_011519640.1:n.-588T>A
XM_011521339.1:c.-469T>A	XP_011519641.1:n.-469T>A
XM_011521340.1:c.-410T>A	XP_011519642.1:n.-410T>A
XM_011521343.1:c.-672T>A	XP_011519645.1:n.-672T>A
XM_011521345.1:c.-643T>A	XP_011519647.1:n.-643T>A
XM_011521338.3:c.-588T>A	XP_011519640.1:n.-588T>A
XM_011521339.3:c.-469T>A	XP_011519641.1:n.-469T>A
XM_011521340.3:c.-410T>A	XP_011519642.1:n.-410T>A
XM_011521343.3:c.-672T>A	XP_011519645.1:n.-672T>A
XM_011521345.3:c.-643T>A	XP_011519647.1:n.-643T>A
NM_001387260.1:c.-98T>A	NP_001374189.1:n.-98T>A