Canonical Allele Identifier: CA2628214314

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711352-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711352T>A , CM000677.2:g.44711352T>A	GRCh38
NC_000015.9:g.45003550T>A , CM000677.1:g.45003550T>A	GRCh37
NC_000015.8:g.42790842T>A	NCBI36
NG_012920.1:g.4866T>A
NG_012920.2:g.4876T>A

Transcript Alleles

HGVS	Amino-acid Change
XM_011521338.1:c.-586A>T	XP_011519640.1:n.-586A>T
XM_011521339.1:c.-467A>T	XP_011519641.1:n.-467A>T
XM_011521340.1:c.-408A>T	XP_011519642.1:n.-408A>T
XM_011521343.1:c.-670A>T	XP_011519645.1:n.-670A>T
XM_011521345.1:c.-641A>T	XP_011519647.1:n.-641A>T
XM_011521338.3:c.-586A>T	XP_011519640.1:n.-586A>T
XM_011521339.3:c.-467A>T	XP_011519641.1:n.-467A>T
XM_011521340.3:c.-408A>T	XP_011519642.1:n.-408A>T
XM_011521343.3:c.-670A>T	XP_011519645.1:n.-670A>T
XM_011521345.3:c.-641A>T	XP_011519647.1:n.-641A>T
NM_001387260.1:c.-96A>T	NP_001374189.1:n.-96A>T