Canonical Allele Identifier: CA490206206

Gene: PATL2

Linked Data

• MyVariant Identifiers: chr15:g.45003297A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711099A>T , CM000677.2:g.44711099A>T	GRCh38
NC_000015.9:g.45003297A>T , CM000677.1:g.45003297A>T	GRCh37
NC_000015.8:g.42790589A>T	NCBI36
NG_012920.1:g.4613A>T
NG_012920.2:g.4623A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-333T>A MANE Select	ENSP00000508024.1:n.-333T>A
ENST00000558573.1:n.218T>A
XM_011521338.1:c.-333T>A	XP_011519640.1:n.-333T>A
XM_011521339.1:c.-214T>A	XP_011519641.1:n.-214T>A
XM_011521340.1:c.-155T>A	XP_011519642.1:n.-155T>A
XM_011521343.1:c.-417T>A	XP_011519645.1:n.-417T>A
XM_011521345.1:c.-388T>A	XP_011519647.1:n.-388T>A
XM_011521338.3:c.-333T>A	XP_011519640.1:n.-333T>A
XM_011521339.3:c.-214T>A	XP_011519641.1:n.-214T>A
XM_011521340.3:c.-155T>A	XP_011519642.1:n.-155T>A
XM_011521343.3:c.-417T>A	XP_011519645.1:n.-417T>A
XM_011521345.3:c.-388T>A	XP_011519647.1:n.-388T>A
NM_001387260.1:c.-76+233T>A	NP_001374189.1:n.-76+233T>A
NM_001387261.1:c.-155T>A	NP_001374190.1:n.-155T>A
NM_001387262.1:c.-423T>A	NP_001374191.1:n.-423T>A
NM_001387263.1:c.-333T>A MANE Select	NP_001374192.1:n.-333T>A