Canonical Allele Identifier: CA9017767

Gene: BSG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.579514A>G , CM000681.2:g.579514A>G	GRCh38
NC_000019.9:g.579514A>G , CM000681.1:g.579514A>G	GRCh37
NC_000019.8:g.530514A>G	NCBI36
NG_007468.1:g.13190A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333511.9:c.430A>G MANE Select	ENSP00000333769.3:p.Thr144Ala
ENST00000346916.9:c.-55-865A>G	ENSP00000344707.4:n.-55-865A>G
ENST00000353555.9:c.82A>G	ENSP00000343809.4:p.Thr28Ala
ENST00000571735.3:n.665A>G
ENST00000572899.6:n.123A>G
ENST00000573784.6:c.-198A>G	ENSP00000473393.2:n.-198A>G
ENST00000576925.4:n.145A>G
ENST00000576984.3:c.-198A>G	ENSP00000473528.2:n.-198A>G
ENST00000613627.5:c.68-865A>G	ENSP00000484849.2:n.68-865A>G
ENST00000618112.4:c.82A>G	ENSP00000495088.2:p.Thr28Ala
ENST00000679472.1:c.-198A>G	ENSP00000505067.1:n.-198A>G
ENST00000680065.1:c.-198A>G	ENSP00000506020.1:n.-198A>G
ENST00000680326.1:c.73A>G	ENSP00000505863.1:p.Thr25Ala
ENST00000680552.1:c.82A>G	ENSP00000506321.1:p.Thr28Ala
ENST00000333511.7:c.430A>G	ENSP00000333769.3:p.Thr144Ala
ENST00000346916.8:c.33-865A>G	ENSP00000344707.3:n.33-865A>G
ENST00000353555.8:c.82A>G	ENSP00000343809.4:p.Thr28Ala
ENST00000545507.6:c.-198A>G	ENSP00000473664.1:n.-198A>G
ENST00000571735.2:n.679A>G
ENST00000572899.5:n.123A>G
ENST00000573216.5:c.68-10A>G	ENSP00000458665.1:n.68-10A>G
ENST00000573784.5:c.-198A>G	ENSP00000473393.1:n.-198A>G
ENST00000574970.2:n.455A>G
ENST00000576925.3:n.145A>G
ENST00000576984.2:c.-198A>G	ENSP00000473528.1:n.-198A>G
ENST00000613627.4:c.73A>G	ENSP00000484849.1:p.Thr25Ala
ENST00000614867.2:c.82A>G	ENSP00000484624.1:p.Thr28Ala
ENST00000618006.4:c.68-1132A>G	ENSP00000478958.1:n.68-1132A>G
NM_001728.3:c.430A>G	NP_001719.2:p.Thr144Ala
NM_198589.2:c.82A>G	NP_940991.1:p.Thr28Ala
NM_198590.2:c.-198A>G	NP_940992.1:n.-198A>G
NM_198591.2:c.33-865A>G	NP_940993.1:n.33-865A>G
XM_005259619.1:c.82A>G	XP_005259676.1:p.Thr28Ala
NM_001322243.1:c.82A>G	NP_001309172.1:p.Thr28Ala
XM_017027173.2:c.430A>G	XP_016882662.1:p.Thr144Ala
NM_001322243.2:c.82A>G	NP_001309172.1:p.Thr28Ala
NM_001728.4:c.430A>G MANE Select	NP_001719.2:p.Thr144Ala
NM_198589.3:c.82A>G	NP_940991.1:p.Thr28Ala
NM_198590.3:c.-198A>G	NP_940992.1:n.-198A>G
NM_198591.3:c.33-865A>G	NP_940993.1:n.33-865A>G
NM_198591.4:c.-55-865A>G	NP_940993.2:n.-55-865A>G