Canonical Allele Identifier: CA1617063167

Gene: BTN2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.26458037T= , CM000668.2:g.26458037T=	GRCh38
NC_000006.11:g.26458265T= , CM000668.1:g.26458265T=	GRCh37
NC_000006.10:g.26566244T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312541.10:c.-136T= MANE Select	ENSP00000312158.5:n.-136T=
ENST00000377600.7:c.-136T=	ENSP00000366825.2:n.-136T=
ENST00000312541.9:c.-136T=	ENSP00000312158.5:n.-136T=
ENST00000377600.6:c.-136T=	ENSP00000366825.2:n.-136T=
ENST00000429381.5:c.-136T=	ENSP00000416945.1:n.-136T=
ENST00000469185.5:c.-136T=	ENSP00000419043.1:n.-136T=
ENST00000493173.1:c.-207T=	ENSP00000420447.1:n.-207T=
ENST00000541522.5:c.-207T=	ENSP00000443909.1:n.-207T=
NM_001197233.2:c.-207T=	NP_001184162.1:n.-207T=
NM_001197234.2:c.-136T=	NP_001184163.1:n.-136T=
NM_007049.4:c.-136T=	NP_008980.1:n.-136T=
NM_078476.3:c.-136T=	NP_510961.1:n.-136T=
NM_007049.5:c.-136T= MANE Select	NP_008980.1:n.-136T=
NM_001197234.3:c.-136T=	NP_001184163.1:n.-136T=
NM_078476.4:c.-136T=	NP_510961.1:n.-136T=
NM_001197233.3:c.-207T=	NP_001184162.1:n.-207T=