Canonical Allele Identifier: CA387501563
Gene: SGCG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23250652C>A , CM000675.2:g.23250652C>A GRCh38
NC_000013.10:g.23824791C>A , CM000675.1:g.23824791C>A GRCh37
NC_000013.9:g.22722791C>A NCBI36
NG_008759.1:g.74732C>A , LRG_207:g.74732C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218867.4:c.320C>A MANE Select ENSP00000218867.3:p.Ser107Ter
ENST00000218867.3:c.320C>A ENSP00000218867.3:p.Ser107Ter
NM_000231.2:c.320C>A , LRG_207t1:c.320C>A NP_000222.1:p.Ser107Ter
XM_005266505.2:c.320C>A XP_005266562.1:p.Ser107Ter
XM_006719861.2:c.374C>A XP_006719924.1:p.Ser125Ter
XM_006719861.3:c.374C>A XP_006719924.1:p.Ser125Ter
XM_024449397.1:c.320C>A XP_024305165.1:p.Ser107Ter
NM_000231.3:c.320C>A MANE Select NP_000222.2:p.Ser107Ter
NM_001378244.1:c.374C>A NP_001365173.1:p.Ser125Ter
NM_001378245.1:c.320C>A NP_001365174.1:p.Ser107Ter
NM_001378246.1:c.320C>A NP_001365175.1:p.Ser107Ter