Canonical Allele Identifier: CA2838503498

Gene: BTNL8

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180950589T>C , CM000667.2:g.180950589T>C	GRCh38
NC_000005.9:g.180377589T>C , CM000667.1:g.180377589T>C	GRCh37
NC_000005.8:g.180310195T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340184.9:c.*45T>C MANE Select	ENSP00000342197.4:n.*45T>C
ENST00000231229.8:c.*634T>C	ENSP00000231229.4:n.*634T>C
ENST00000340184.8:c.*45T>C	ENSP00000342197.4:n.*45T>C
ENST00000400707.7:c.*45T>C	ENSP00000383543.3:n.*45T>C
ENST00000505126.5:c.*45T>C	ENSP00000427441.1:n.*45T>C
ENST00000508408.5:c.*634T>C	ENSP00000424585.1:n.*634T>C
ENST00000511704.5:c.*45T>C	ENSP00000425207.1:n.*45T>C
ENST00000533815.2:c.*45T>C	ENSP00000435098.2:n.*45T>C
ENST00000610640.4:c.1173T>C	ENSP00000483717.1:n.1173T>C
NM_001040462.2:c.*45T>C	NP_001035552.1:n.*45T>C
NM_001159707.1:c.*45T>C	NP_001153179.1:n.*45T>C
NM_001159708.1:c.*634T>C	NP_001153180.1:n.*634T>C
NM_001159709.1:c.*45T>C	NP_001153181.1:n.*45T>C
NM_001159710.1:c.*45T>C	NP_001153182.1:n.*45T>C
NM_024850.2:c.*634T>C	NP_079126.1:n.*634T>C
XM_011534649.1:c.*45T>C	XP_011532951.1:n.*45T>C
XM_011534650.1:c.*45T>C	XP_011532952.1:n.*45T>C
XM_011534651.1:c.*45T>C	XP_011532953.1:n.*45T>C
XM_011534652.1:c.*45T>C	XP_011532954.1:n.*45T>C
XM_011534653.1:c.*45T>C	XP_011532955.1:n.*45T>C
XM_011534649.2:c.*45T>C	XP_011532951.1:n.*45T>C
XM_011534650.2:c.*45T>C	XP_011532952.1:n.*45T>C
XM_011534651.3:c.*45T>C	XP_011532953.1:n.*45T>C
XM_011534652.3:c.*45T>C	XP_011532954.1:n.*45T>C
XM_011534653.2:c.*45T>C	XP_011532955.1:n.*45T>C
NM_001040462.3:c.*45T>C MANE Select	NP_001035552.1:n.*45T>C
NM_001159707.2:c.*45T>C	NP_001153179.1:n.*45T>C
NM_001159708.2:c.*634T>C	NP_001153180.1:n.*634T>C
NM_001159709.2:c.*45T>C	NP_001153181.1:n.*45T>C
NM_001159710.2:c.*45T>C	NP_001153182.1:n.*45T>C
NM_024850.3:c.*634T>C	NP_079126.1:n.*634T>C