Canonical Allele Identifier: CA490205949

Gene: PATL2

Linked Data

• MyVariant Identifiers: chr15:g.45003233A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711035A>T , CM000677.2:g.44711035A>T	GRCh38
NC_000015.9:g.45003233A>T , CM000677.1:g.45003233A>T	GRCh37
NC_000015.8:g.42790525A>T	NCBI36
NG_012920.1:g.4549A>T
NG_012920.2:g.4559A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-269T>A MANE Select	ENSP00000508024.1:n.-269T>A
ENST00000558573.1:n.282T>A
XM_011521338.1:c.-269T>A	XP_011519640.1:n.-269T>A
XM_011521339.1:c.-150T>A	XP_011519641.1:n.-150T>A
XM_011521340.1:c.-91T>A	XP_011519642.1:n.-91T>A
XM_011521343.1:c.-353T>A	XP_011519645.1:n.-353T>A
XM_011521345.1:c.-324T>A	XP_011519647.1:n.-324T>A
XM_011521338.3:c.-269T>A	XP_011519640.1:n.-269T>A
XM_011521339.3:c.-150T>A	XP_011519641.1:n.-150T>A
XM_011521340.3:c.-91T>A	XP_011519642.1:n.-91T>A
XM_011521343.3:c.-353T>A	XP_011519645.1:n.-353T>A
XM_011521345.3:c.-324T>A	XP_011519647.1:n.-324T>A
NM_001387260.1:c.-76+297T>A	NP_001374189.1:n.-76+297T>A
NM_001387261.1:c.-91T>A	NP_001374190.1:n.-91T>A
NM_001387262.1:c.-359T>A	NP_001374191.1:n.-359T>A
NM_001387263.1:c.-269T>A MANE Select	NP_001374192.1:n.-269T>A