Canonical Allele Identifier: CA490206342

Gene: PATL2

Linked Data

• MyVariant Identifiers: chr15:g.45003332A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711134A>T , CM000677.2:g.44711134A>T	GRCh38
NC_000015.9:g.45003332A>T , CM000677.1:g.45003332A>T	GRCh37
NC_000015.8:g.42790624A>T	NCBI36
NG_012920.1:g.4648A>T
NG_012920.2:g.4658A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-368T>A MANE Select	ENSP00000508024.1:n.-368T>A
ENST00000558573.1:n.183T>A
XM_011521338.1:c.-368T>A	XP_011519640.1:n.-368T>A
XM_011521339.1:c.-249T>A	XP_011519641.1:n.-249T>A
XM_011521340.1:c.-190T>A	XP_011519642.1:n.-190T>A
XM_011521343.1:c.-452T>A	XP_011519645.1:n.-452T>A
XM_011521345.1:c.-423T>A	XP_011519647.1:n.-423T>A
XM_011521338.3:c.-368T>A	XP_011519640.1:n.-368T>A
XM_011521339.3:c.-249T>A	XP_011519641.1:n.-249T>A
XM_011521340.3:c.-190T>A	XP_011519642.1:n.-190T>A
XM_011521343.3:c.-452T>A	XP_011519645.1:n.-452T>A
XM_011521345.3:c.-423T>A	XP_011519647.1:n.-423T>A
NM_001387260.1:c.-76+198T>A	NP_001374189.1:n.-76+198T>A
NM_001387261.1:c.-190T>A	NP_001374190.1:n.-190T>A
NM_001387262.1:c.-458T>A	NP_001374191.1:n.-458T>A
NM_001387263.1:c.-368T>A MANE Select	NP_001374192.1:n.-368T>A