Canonical Allele Identifier: CA490206813

Gene: PATL2

Linked Data

• MyVariant Identifiers: chr15:g.45003487C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711289C>G , CM000677.2:g.44711289C>G	GRCh38
NC_000015.9:g.45003487C>G , CM000677.1:g.45003487C>G	GRCh37
NC_000015.8:g.42790779C>G	NCBI36
NG_012920.1:g.4803C>G
NG_012920.2:g.4813C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-523G>C MANE Select	ENSP00000508024.1:n.-523G>C
ENST00000558573.1:n.28G>C
XM_011521338.1:c.-523G>C	XP_011519640.1:n.-523G>C
XM_011521339.1:c.-404G>C	XP_011519641.1:n.-404G>C
XM_011521340.1:c.-345G>C	XP_011519642.1:n.-345G>C
XM_011521343.1:c.-607G>C	XP_011519645.1:n.-607G>C
XM_011521345.1:c.-578G>C	XP_011519647.1:n.-578G>C
XM_011521338.3:c.-523G>C	XP_011519640.1:n.-523G>C
XM_011521339.3:c.-404G>C	XP_011519641.1:n.-404G>C
XM_011521340.3:c.-345G>C	XP_011519642.1:n.-345G>C
XM_011521343.3:c.-607G>C	XP_011519645.1:n.-607G>C
XM_011521345.3:c.-578G>C	XP_011519647.1:n.-578G>C
NM_001387260.1:c.-76+43G>C	NP_001374189.1:n.-76+43G>C
NM_001387261.1:c.-345G>C	NP_001374190.1:n.-345G>C
NM_001387262.1:c.-613G>C	NP_001374191.1:n.-613G>C
NM_001387263.1:c.-523G>C MANE Select	NP_001374192.1:n.-523G>C