Canonical Allele Identifier: CA2395240004

Gene: BID

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.17743998T= , CM000684.2:g.17743998T=	GRCh38
NC_000022.10:g.18226764T= , CM000684.1:g.18226764T=	GRCh37
NC_000022.9:g.16606764T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001196.4:c.28A= MANE Select	NP_001187.1:p.Ser10=
ENST00000622694.5:c.28A= MANE Select	ENSP00000480414.1:p.Ser10=
NM_001196.3:c.28A=	NP_001187.1:p.Ser10=
NM_001244567.1:c.28A=	NP_001231496.1:p.Ser10=
NM_001244569.1:c.-65-4510A=	NP_001231498.1:n.-65-4510A=
NM_001244570.1:c.-65-4510A=	NP_001231499.1:n.-65-4510A=
NM_001244572.1:c.-65-4510A=	NP_001231501.1:n.-65-4510A=
NM_197966.2:c.166A=	NP_932070.1:p.Ser56=
NM_197966.3:c.166A=	NP_932070.1:p.Ser56=
NM_197967.2:c.-261A=	NP_932071.1:n.-261A=
ENST00000317361.11:c.166A=	ENSP00000318822.7:p.Ser56=
ENST00000342111.9:c.28A=	ENSP00000344594.5:p.Ser10=
ENST00000399765.5:c.-65-4510A=	ENSP00000382667.1:n.-65-4510A=
ENST00000399767.5:c.-261A=	ENSP00000382669.1:n.-261A=
ENST00000399767.6:c.-261A=	ENSP00000382669.1:n.-261A=
ENST00000399774.7:c.28A=	ENSP00000382674.3:p.Ser10=
ENST00000473439.5:n.131A=
ENST00000550946.5:n.118A=
ENST00000551952.5:c.28A=	ENSP00000449236.1:p.Ser10=
ENST00000552886.1:n.94A=
ENST00000611040.1:c.-65-4510A=	ENSP00000483709.1:n.-65-4510A=
ENST00000614949.4:c.-65-4510A=	ENSP00000477773.1:n.-65-4510A=
ENST00000615414.4:c.-65-4510A=	ENSP00000483534.1:n.-65-4510A=
ENST00000617586.1:c.28A=	ENSP00000481991.1:p.Ser10=
ENST00000622694.4:c.28A=	ENSP00000480414.1:p.Ser10=