Canonical Allele Identifier: CA401928282

Gene: GNAL

Linked Data

• MyVariant Identifiers: chr18:g.11881054A>C (hg19) ; chr18:g.11881055A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.11881055A>C , CM000680.2:g.11881055A>C	GRCh38
NC_000018.9:g.11881054A>C , CM000680.1:g.11881054A>C	GRCh37
NC_000018.8:g.11871054A>C	NCBI36
NG_033866.1:g.197041A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000334049.11:c.1297A>C MANE Select	ENSP00000334051.5:p.Thr433Pro
ENST00000423027.8:c.1066A>C MANE Plus Clinical	ENSP00000408489.2:p.Thr356Pro
ENST00000269162.9:c.1066A>C	ENSP00000269162.4:p.Thr356Pro
ENST00000334049.10:c.1297A>C	ENSP00000334051.5:p.Thr433Pro
ENST00000423027.7:c.1066A>C	ENSP00000408489.2:p.Thr356Pro
ENST00000535121.5:c.1066A>C	ENSP00000439023.1:p.Thr356Pro
ENST00000602628.1:c.445A>C	ENSP00000473600.1:p.Thr149Pro
NM_001142339.2:c.1066A>C	NP_001135811.1:p.Thr356Pro
NM_001261443.1:c.1066A>C	NP_001248372.1:p.Thr356Pro
NM_001261444.1:c.445A>C	NP_001248373.1:p.Thr149Pro
NM_182978.3:c.1297A>C	NP_892023.1:p.Thr433Pro
XM_006722323.2:c.1066A>C	XP_006722386.1:p.Thr356Pro
XM_011525654.1:c.1066A>C	XP_011523956.1:p.Thr356Pro
XM_024451164.1:c.1066A>C	XP_024306932.1:p.Thr356Pro
NM_182978.4:c.1297A>C MANE Select	NP_892023.1:p.Thr433Pro
NM_001261444.2:c.445A>C	NP_001248373.1:p.Thr149Pro
NM_001369387.1:c.1066A>C MANE Plus Clinical	NP_001356316.1:p.Thr356Pro
NM_001142339.3:c.1066A>C	NP_001135811.1:p.Thr356Pro
NM_001261443.2:c.1066A>C	NP_001248372.1:p.Thr356Pro