Canonical Allele Identifier: CA8893953

Gene: GNAL

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.11824887T>G , CM000680.2:g.11824887T>G	GRCh38
NC_000018.9:g.11824886T>G , CM000680.1:g.11824886T>G	GRCh37
NC_000018.8:g.11814886T>G	NCBI36
NG_033866.1:g.140873T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_182978.4:c.625-31T>G MANE Select	NP_892023.1:n.625-31T>G
ENST00000334049.11:c.625-31T>G MANE Select	ENSP00000334051.5:n.625-31T>G
NM_001369387.1:c.394-31T>G MANE Plus Clinical	NP_001356316.1:n.394-31T>G
ENST00000423027.8:c.394-31T>G MANE Plus Clinical	ENSP00000408489.2:n.394-31T>G
NM_001142339.2:c.394-31T>G	NP_001135811.1:n.394-31T>G
NM_001142339.3:c.394-31T>G	NP_001135811.1:n.394-31T>G
NM_001261443.1:c.394-31T>G	NP_001248372.1:n.394-31T>G
NM_001261443.2:c.394-31T>G	NP_001248372.1:n.394-31T>G
NM_182978.3:c.625-31T>G	NP_892023.1:n.625-31T>G
ENST00000269162.9:c.394-31T>G	ENSP00000269162.4:n.394-31T>G
ENST00000334049.10:c.625-31T>G	ENSP00000334051.5:n.625-31T>G
ENST00000423027.7:c.394-31T>G	ENSP00000408489.2:n.394-31T>G
ENST00000535121.5:c.394-31T>G	ENSP00000439023.1:n.394-31T>G
ENST00000585642.5:c.211-31T>G	ENSP00000467345.1:n.211-31T>G
ENST00000590228.1:c.106-31T>G	ENSP00000467709.1:n.106-31T>G
ENST00000590972.1:n.218-31T>G
XM_006722323.2:c.394-31T>G	XP_006722386.1:n.394-31T>G
XM_006722324.1:c.625-31T>G	XP_006722387.1:n.625-31T>G
XM_006722324.3:c.625-31T>G	XP_006722387.1:n.625-31T>G
XM_011525654.1:c.394-31T>G	XP_011523956.1:n.394-31T>G
XM_024451164.1:c.394-31T>G	XP_024306932.1:n.394-31T>G