Canonical Allele Identifier: CA387501684
Gene: SGCG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23250711A>T , CM000675.2:g.23250711A>T GRCh38
NC_000013.10:g.23824850A>T , CM000675.1:g.23824850A>T GRCh37
NC_000013.9:g.22722850A>T NCBI36
NG_008759.1:g.74791A>T , LRG_207:g.74791A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000218867.4:c.379A>T MANE Select ENSP00000218867.3:p.Lys127Ter
ENST00000218867.3:c.379A>T ENSP00000218867.3:p.Lys127Ter
NM_000231.2:c.379A>T , LRG_207t1:c.379A>T NP_000222.1:p.Lys127Ter
XM_005266505.2:c.379A>T XP_005266562.1:p.Lys127Ter
XM_006719861.2:c.433A>T XP_006719924.1:p.Lys145Ter
XM_006719861.3:c.433A>T XP_006719924.1:p.Lys145Ter
XM_024449397.1:c.379A>T XP_024305165.1:p.Lys127Ter
NM_000231.3:c.379A>T MANE Select NP_000222.2:p.Lys127Ter
NM_001378244.1:c.433A>T NP_001365173.1:p.Lys145Ter
NM_001378245.1:c.379A>T NP_001365174.1:p.Lys127Ter
NM_001378246.1:c.379A>T NP_001365175.1:p.Lys127Ter