Canonical Allele Identifier: CA1457429104
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027955_52027958delinsAAAG , CM000666.2:g.52027955_52027958delinsAAAG GRCh38
NC_000004.11:g.52894121_52894124delinsAAAG , CM000666.1:g.52894121_52894124delinsAAAG GRCh37
NC_000004.10:g.52588878_52588881delinsAAAG NCBI36
NG_008891.1:g.15362_15365delinsCTTT , LRG_204:g.15362_15365delinsCTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.753+10_753+13delinsCTTT MANE Select ENSP00000370839.6:n.753+10_753+13delinsCT...
ENST00000381431.9:c.753+10_753+13delinsCTTT ENSP00000370839.5:n.753+10_753+13delinsCT...
NM_000232.4:c.753+10_753+13delinsCTTT , LRG_204t1:c.753+10_753+13delinsCTTT NP_000223.1:n.753+10_753+13delinsCTTT
XM_006714049.2:c.456+10_456+13delinsCTTT XP_006714112.1:n.456+10_456+13delinsCTTT
XM_011534403.1:c.543+10_543+13delinsCTTT XP_011532705.1:n.543+10_543+13delinsCTTT
XM_011534404.1:c.456+10_456+13delinsCTTT XP_011532706.1:n.456+10_456+13delinsCTTT
NM_000232.5:c.753+10_753+13delinsCTTT MANE Select NP_000223.1:n.753+10_753+13delinsCTTT