Canonical Allele Identifier: CA130676
Gene: GNAL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.11752494C>T , CM000680.2:g.11752494C>T GRCh38
NC_000018.9:g.11752493C>T , CM000680.1:g.11752493C>T GRCh37
NC_000018.8:g.11742493C>T NCBI36
NG_033866.1:g.68480C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000334049.11:c.377-359C>T MANE Select ENSP00000334051.5:n.377-359C>T
ENST00000423027.8:c.61C>T MANE Plus Clinical ENSP00000408489.2:p.Arg21Ter
ENST00000269162.9:c.61C>T ENSP00000269162.4:p.Arg21Ter
ENST00000334049.10:c.377-359C>T ENSP00000334051.5:n.377-359C>T
ENST00000423027.7:c.61C>T ENSP00000408489.2:p.Arg21Ter
ENST00000535121.5:c.61C>T ENSP00000439023.1:p.Arg21Ter
NM_001142339.2:c.61C>T NP_001135811.1:p.Arg21Ter
NM_001261443.1:c.61C>T NP_001248372.1:p.Arg21Ter
NM_182978.3:c.377-359C>T NP_892023.1:n.377-359C>T
XM_006722323.2:c.61C>T XP_006722386.1:p.Arg21Ter
XM_006722324.1:c.377-359C>T XP_006722387.1:n.377-359C>T
XM_011525654.1:c.61C>T XP_011523956.1:p.Arg21Ter
XM_006722324.3:c.377-359C>T XP_006722387.1:n.377-359C>T
XM_024451164.1:c.61C>T XP_024306932.1:p.Arg21Ter
NM_182978.4:c.377-359C>T MANE Select NP_892023.1:n.377-359C>T
NM_001369387.1:c.61C>T MANE Plus Clinical NP_001356316.1:p.Arg21Ter
NM_001142339.3:c.61C>T NP_001135811.1:p.Arg21Ter
NM_001261443.2:c.61C>T NP_001248372.1:p.Arg21Ter
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