Canonical Allele Identifier: CA2317189241
Gene: BSG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.580238_580241delinsCAGG , CM000681.2:g.580238_580241delinsCAGG GRCh38
NC_000019.9:g.580238_580241delinsCAGG , CM000681.1:g.580238_580241delinsCAGG GRCh37
NC_000019.8:g.531238_531241delinsCAGG NCBI36
NG_007468.1:g.13914_13917delinsCAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000333511.9:c.573-141_573-138delinsCAGG MANE Select ENSP00000333769.3:n.573-141_573-138delinsCAGG
ENST00000346916.9:c.-55-141_-55-138delinsCAGG ENSP00000344707.4:n.-55-141_-55-138delinsCAGG
ENST00000353555.9:c.225-141_225-138delinsCAGG ENSP00000343809.4:n.225-141_225-138delinsCAGG
ENST00000571735.3:n.808-141_808-138delinsCAGG
ENST00000572899.6:n.266-141_266-138delinsCAGG
ENST00000573784.6:c.-55-141_-55-138delinsCAGG ENSP00000473393.2:n.-55-141_-55-138delinsCAGG
ENST00000576925.4:n.869_872delinsCAGG
ENST00000576984.3:c.-55-141_-55-138delinsCAGG ENSP00000473528.2:n.-55-141_-55-138delinsCAGG
ENST00000613627.5:c.68-141_68-138delinsCAGG ENSP00000484849.2:n.68-141_68-138delinsCAGG
ENST00000618112.4:c.225-141_225-138delinsCAGG ENSP00000495088.2:n.225-141_225-138delinsCAGG
ENST00000679472.1:c.-55-141_-55-138delinsCAGG ENSP00000505067.1:n.-55-141_-55-138delinsCAGG
ENST00000680065.1:c.-55-141_-55-138delinsCAGG ENSP00000506020.1:n.-55-141_-55-138delinsCAGG
ENST00000680326.1:c.216-141_216-138delinsCAGG ENSP00000505863.1:n.216-141_216-138delinsCAGG
ENST00000680552.1:c.225-141_225-138delinsCAGG ENSP00000506321.1:n.225-141_225-138delinsCAGG
ENST00000333511.7:c.573-141_573-138delinsCAGG ENSP00000333769.3:n.573-141_573-138delinsCAGG
ENST00000346916.8:c.33-141_33-138delinsCAGG ENSP00000344707.3:n.33-141_33-138delinsCAGG
ENST00000353555.8:c.225-141_225-138delinsCAGG ENSP00000343809.4:n.225-141_225-138delinsCAGG
ENST00000545507.6:c.-55-141_-55-138delinsCAGG ENSP00000473664.1:n.-55-141_-55-138delinsCAGG
ENST00000571735.2:n.822-141_822-138delinsCAGG
ENST00000572899.5:n.266-141_266-138delinsCAGG
ENST00000573216.5:c.201-141_201-138delinsCAGG ENSP00000458665.1:n.201-141_201-138delinsCAGG
ENST00000573784.5:c.-55-141_-55-138delinsCAGG ENSP00000473393.1:n.-55-141_-55-138delinsCAGG
ENST00000576984.2:c.-55-141_-55-138delinsCAGG ENSP00000473528.1:n.-55-141_-55-138delinsCAGG
ENST00000613627.4:c.216-141_216-138delinsCAGG ENSP00000484849.1:n.216-141_216-138delinsCAGG
ENST00000614867.2:c.147+659_147+662delinsCAGG ENSP00000484624.1:n.147+659_147+662delinsCAGG
ENST00000618006.4:c.68-408_68-405delinsCAGG ENSP00000478958.1:n.68-408_68-405delinsCAGG
NM_001728.3:c.573-141_573-138delinsCAGG NP_001719.2:n.573-141_573-138delinsCAGG
NM_198589.2:c.225-141_225-138delinsCAGG NP_940991.1:n.225-141_225-138delinsCAGG
NM_198590.2:c.-55-141_-55-138delinsCAGG NP_940992.1:n.-55-141_-55-138delinsCAGG
NM_198591.2:c.33-141_33-138delinsCAGG NP_940993.1:n.33-141_33-138delinsCAGG
XM_005259619.1:c.225-141_225-138delinsCAGG XP_005259676.1:n.225-141_225-138delinsCAGG
NM_001322243.1:c.225-141_225-138delinsCAGG NP_001309172.1:n.225-141_225-138delinsCAGG
XM_017027173.2:c.573-141_573-138delinsCAGG XP_016882662.1:n.573-141_573-138delinsCAGG
NM_001322243.2:c.225-141_225-138delinsCAGG NP_001309172.1:n.225-141_225-138delinsCAGG
NM_001728.4:c.573-141_573-138delinsCAGG MANE Select NP_001719.2:n.573-141_573-138delinsCAGG
NM_198589.3:c.225-141_225-138delinsCAGG NP_940991.1:n.225-141_225-138delinsCAGG
NM_198590.3:c.-55-141_-55-138delinsCAGG NP_940992.1:n.-55-141_-55-138delinsCAGG
NM_198591.3:c.33-141_33-138delinsCAGG NP_940993.1:n.33-141_33-138delinsCAGG
NM_198591.4:c.-55-141_-55-138delinsCAGG NP_940993.2:n.-55-141_-55-138delinsCAGG