Canonical Allele Identifier: CA1457429032
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027817_52027821delinsACTTT , CM000666.2:g.52027817_52027821delinsACTTT GRCh38
NC_000004.11:g.52893983_52893987delinsACTTT , CM000666.1:g.52893983_52893987delinsACTTT GRCh37
NC_000004.10:g.52588740_52588744delinsACTTT NCBI36
NG_008891.1:g.15499_15503delinsAAAGT , LRG_204:g.15499_15503delinsAAAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.753+147_753+151delinsAAAGT MANE Select ENSP00000370839.6:n.753+147_753+151delins...
ENST00000381431.9:c.753+147_753+151delinsAAAGT ENSP00000370839.5:n.753+147_753+151delins...
NM_000232.4:c.753+147_753+151delinsAAAGT , LRG_204t1:c.753+147_753+151delinsAAAGT NP_000223.1:n.753+147_753+151delinsAAAGT
XM_006714049.2:c.456+147_456+151delinsAAAGT XP_006714112.1:n.456+147_456+151delinsAAA...
XM_011534403.1:c.543+147_543+151delinsAAAGT XP_011532705.1:n.543+147_543+151delinsAAA...
XM_011534404.1:c.456+147_456+151delinsAAAGT XP_011532706.1:n.456+147_456+151delinsAAA...
NM_000232.5:c.753+147_753+151delinsAAAGT MANE Select NP_000223.1:n.753+147_753+151delinsAAAGT