Canonical Allele Identifier: CA387501689
Gene: SGCG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23250713A>T , CM000675.2:g.23250713A>T GRCh38
NC_000013.10:g.23824852A>T , CM000675.1:g.23824852A>T GRCh37
NC_000013.9:g.22722852A>T NCBI36
NG_008759.1:g.74793A>T , LRG_207:g.74793A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000218867.4:c.381A>T MANE Select ENSP00000218867.3:p.Lys127Asn
ENST00000218867.3:c.381A>T ENSP00000218867.3:p.Lys127Asn
NM_000231.2:c.381A>T , LRG_207t1:c.381A>T NP_000222.1:p.Lys127Asn
XM_005266505.2:c.381A>T XP_005266562.1:p.Lys127Asn
XM_006719861.2:c.435A>T XP_006719924.1:p.Lys145Asn
XM_006719861.3:c.435A>T XP_006719924.1:p.Lys145Asn
XM_024449397.1:c.381A>T XP_024305165.1:p.Lys127Asn
NM_000231.3:c.381A>T MANE Select NP_000222.2:p.Lys127Asn
NM_001378244.1:c.435A>T NP_001365173.1:p.Lys145Asn
NM_001378245.1:c.381A>T NP_001365174.1:p.Lys127Asn
NM_001378246.1:c.381A>T NP_001365175.1:p.Lys127Asn