Canonical Allele Identifier: CA1594009942

Gene: HAVCR1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157058359C= , CM000667.2:g.157058359C=	GRCh38
NC_000005.9:g.156485370C= , CM000667.1:g.156485370C=	GRCh37
NC_000005.8:g.156417948C=	NCBI36
NG_017001.1:g.5601G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001173393.3:c.-12-404G= MANE Select	NP_001166864.1:n.-12-404G=
ENST00000523175.6:c.-12-404G= MANE Select	ENSP00000427898.1:n.-12-404G=
NM_001099414.1:c.-68G=	NP_001092884.1:n.-68G=
NM_001173393.1:c.-12-404G=	NP_001166864.1:n.-12-404G=
NM_001173393.2:c.-12-404G=	NP_001166864.1:n.-12-404G=
NM_001308156.1:c.-133-283G=	NP_001295085.1:n.-133-283G=
NM_001308156.2:c.-133-283G=	NP_001295085.1:n.-133-283G=
NM_012206.2:c.-416G=	NP_036338.2:n.-416G=
ENST00000339252.7:c.-416G=	ENSP00000344844.3:n.-416G=
ENST00000339252.8:c.-416G=	ENSP00000344844.3:n.-416G=
ENST00000518745.1:c.-68G=	ENSP00000428422.1:n.-68G=
ENST00000522693.5:c.-133-283G=	ENSP00000428524.1:n.-133-283G=
ENST00000523175.5:c.-12-404G=	ENSP00000427898.1:n.-12-404G=
ENST00000625904.2:c.-416G=	ENSP00000487363.1:n.-416G=
ENST00000698790.1:c.-68G=	ENSP00000513932.1:n.-68G=
ENST00000699093.1:c.-12-404G=	ENSP00000514125.1:n.-12-404G=
XM_011534509.1:c.-136-280G=	XP_011532811.1:n.-136-280G=
XM_011534511.1:c.-133-283G=	XP_011532813.1:n.-133-283G=
XM_011534512.1:c.-12-404G=	XP_011532814.1:n.-12-404G=
XM_011534513.1:c.-12-404G=	XP_011532815.1:n.-12-404G=
XM_017009339.2:c.-136-280G=	XP_016864828.1:n.-136-280G=
XM_024446019.1:c.-136-280G=	XP_024301787.1:n.-136-280G=
XM_024446020.1:c.-136-280G=	XP_024301788.1:n.-136-280G=
XM_024446021.1:c.-133-283G=	XP_024301789.1:n.-133-283G=
XM_024446022.1:c.-12-404G=	XP_024301790.1:n.-12-404G=
XM_024446023.1:c.-12-404G=	XP_024301791.1:n.-12-404G=
XM_024446024.1:c.-136-280G=	XP_024301792.1:n.-136-280G=