Canonical Allele Identifier: CA490206205

Gene: PATL2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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