Canonical Allele Identifier: CA490206268

Gene: PATL2

Linked Data

• MyVariant Identifiers: chr15:g.45003313T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711115T>G , CM000677.2:g.44711115T>G	GRCh38
NC_000015.9:g.45003313T>G , CM000677.1:g.45003313T>G	GRCh37
NC_000015.8:g.42790605T>G	NCBI36
NG_012920.1:g.4629T>G
NG_012920.2:g.4639T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-349A>C MANE Select	ENSP00000508024.1:n.-349A>C
ENST00000558573.1:n.202A>C
XM_011521338.1:c.-349A>C	XP_011519640.1:n.-349A>C
XM_011521339.1:c.-230A>C	XP_011519641.1:n.-230A>C
XM_011521340.1:c.-171A>C	XP_011519642.1:n.-171A>C
XM_011521343.1:c.-433A>C	XP_011519645.1:n.-433A>C
XM_011521345.1:c.-404A>C	XP_011519647.1:n.-404A>C
XM_011521338.3:c.-349A>C	XP_011519640.1:n.-349A>C
XM_011521339.3:c.-230A>C	XP_011519641.1:n.-230A>C
XM_011521340.3:c.-171A>C	XP_011519642.1:n.-171A>C
XM_011521343.3:c.-433A>C	XP_011519645.1:n.-433A>C
XM_011521345.3:c.-404A>C	XP_011519647.1:n.-404A>C
NM_001387260.1:c.-76+217A>C	NP_001374189.1:n.-76+217A>C
NM_001387261.1:c.-171A>C	NP_001374190.1:n.-171A>C
NM_001387262.1:c.-439A>C	NP_001374191.1:n.-439A>C
NM_001387263.1:c.-349A>C MANE Select	NP_001374192.1:n.-349A>C