Canonical Allele Identifier: CA2813222653

Gene: BSG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.580246_580248del , CM000681.2:g.580246_580248del	GRCh38
NC_000019.9:g.580246_580248del , CM000681.1:g.580246_580248del	GRCh37
NC_000019.8:g.531246_531248del	NCBI36
NG_007468.1:g.13922_13924del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333511.9:c.573-133_573-131del MANE Select	ENSP00000333769.3:n.573-133_573-131del
ENST00000346916.9:c.-55-133_-55-131del	ENSP00000344707.4:n.-55-133_-55-131del
ENST00000353555.9:c.225-133_225-131del	ENSP00000343809.4:n.225-133_225-131del
ENST00000571735.3:n.808-133_808-131del
ENST00000572899.6:n.266-133_266-131del
ENST00000573784.6:c.-55-133_-55-131del	ENSP00000473393.2:n.-55-133_-55-131del
ENST00000576925.4:n.877_879del
ENST00000576984.3:c.-55-133_-55-131del	ENSP00000473528.2:n.-55-133_-55-131del
ENST00000613627.5:c.68-133_68-131del	ENSP00000484849.2:n.68-133_68-131del
ENST00000618112.4:c.225-133_225-131del	ENSP00000495088.2:n.225-133_225-131del
ENST00000679472.1:c.-55-133_-55-131del	ENSP00000505067.1:n.-55-133_-55-131del
ENST00000680065.1:c.-55-133_-55-131del	ENSP00000506020.1:n.-55-133_-55-131del
ENST00000680326.1:c.216-133_216-131del	ENSP00000505863.1:n.216-133_216-131del
ENST00000680552.1:c.225-133_225-131del	ENSP00000506321.1:n.225-133_225-131del
ENST00000333511.7:c.573-133_573-131del	ENSP00000333769.3:n.573-133_573-131del
ENST00000346916.8:c.33-133_33-131del	ENSP00000344707.3:n.33-133_33-131del
ENST00000353555.8:c.225-133_225-131del	ENSP00000343809.4:n.225-133_225-131del
ENST00000545507.6:c.-55-133_-55-131del	ENSP00000473664.1:n.-55-133_-55-131del
ENST00000571735.2:n.822-133_822-131del
ENST00000572899.5:n.266-133_266-131del
ENST00000573216.5:c.201-133_201-131del	ENSP00000458665.1:n.201-133_201-131del
ENST00000573784.5:c.-55-133_-55-131del	ENSP00000473393.1:n.-55-133_-55-131del
ENST00000576984.2:c.-55-133_-55-131del	ENSP00000473528.1:n.-55-133_-55-131del
ENST00000613627.4:c.216-133_216-131del	ENSP00000484849.1:n.216-133_216-131del
ENST00000614867.2:c.147+667_147+669del	ENSP00000484624.1:n.147+667_147+669del
ENST00000618006.4:c.68-400_68-398del	ENSP00000478958.1:n.68-400_68-398del
NM_001728.3:c.573-133_573-131del	NP_001719.2:n.573-133_573-131del
NM_198589.2:c.225-133_225-131del	NP_940991.1:n.225-133_225-131del
NM_198590.2:c.-55-133_-55-131del	NP_940992.1:n.-55-133_-55-131del
NM_198591.2:c.33-133_33-131del	NP_940993.1:n.33-133_33-131del
XM_005259619.1:c.225-133_225-131del	XP_005259676.1:n.225-133_225-131del
NM_001322243.1:c.225-133_225-131del	NP_001309172.1:n.225-133_225-131del
XM_017027173.2:c.573-133_573-131del	XP_016882662.1:n.573-133_573-131del
NM_001322243.2:c.225-133_225-131del	NP_001309172.1:n.225-133_225-131del
NM_001728.4:c.573-133_573-131del MANE Select	NP_001719.2:n.573-133_573-131del
NM_198589.3:c.225-133_225-131del	NP_940991.1:n.225-133_225-131del
NM_198590.3:c.-55-133_-55-131del	NP_940992.1:n.-55-133_-55-131del
NM_198591.3:c.33-133_33-131del	NP_940993.1:n.33-133_33-131del
NM_198591.4:c.-55-133_-55-131del	NP_940993.2:n.-55-133_-55-131del