Canonical Allele Identifier: CA130128350

Gene: HAVCR1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157052413_157052415delinsCGC , CM000667.2:g.157052413_157052415delinsCGC	GRCh38
NC_000005.9:g.156479424_156479426delinsCGC , CM000667.1:g.156479424_156479426delinsCGC	GRCh37
NC_000005.8:g.156412002_156412004delinsCGC	NCBI36
NG_017001.1:g.11545_11547delinsGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339252.8:c.619_621delinsGCG	ENSP00000344844.3:p.Thr207Ala
ENST00000698790.1:c.619_621delinsGCG	ENSP00000513932.1:p.Thr207Ala
ENST00000699093.1:c.619_621delinsGCG	ENSP00000514125.1:p.Thr207Ala
ENST00000523175.6:c.619_621delinsGCG MANE Select	ENSP00000427898.1:p.Thr207Ala
ENST00000339252.7:c.619_621delinsGCG	ENSP00000344844.3:p.Thr207Ala
ENST00000518745.1:c.619_621delinsGCG	ENSP00000428422.1:p.Thr207Ala
ENST00000522693.5:c.619_621delinsGCG	ENSP00000428524.1:p.Thr207Ala
ENST00000523175.5:c.619_621delinsGCG	ENSP00000427898.1:p.Thr207Ala
ENST00000625904.2:c.619_621delinsGCG	ENSP00000487363.1:p.Thr207Ala
NM_001099414.1:c.619_621delinsGCG	NP_001092884.1:p.Thr207Ala
NM_001173393.1:c.619_621delinsGCG	NP_001166864.1:p.Thr207Ala
NM_001173393.2:c.619_621delinsGCG	NP_001166864.1:p.Thr207Ala
NM_001308156.1:c.619_621delinsGCG	NP_001295085.1:p.Thr207Ala
NM_012206.2:c.619_621delinsGCG	NP_036338.2:p.Thr207Ala
NM_012206.3:c.619_621delinsGCG	NP_036338.2:p.Thr207Ala
XM_006714840.2:c.619_621delinsGCG	XP_006714903.1:p.Thr207Ala
XM_011534508.1:c.619_621delinsGCG	XP_011532810.1:p.Thr207Ala
XM_011534509.1:c.619_621delinsGCG	XP_011532811.1:p.Thr207Ala
XM_011534510.1:c.619_621delinsGCG	XP_011532812.1:p.Thr207Ala
XM_011534511.1:c.619_621delinsGCG	XP_011532813.1:p.Thr207Ala
XM_011534512.1:c.619_621delinsGCG	XP_011532814.1:p.Thr207Ala
XM_011534513.1:c.619_621delinsGCG	XP_011532815.1:p.Thr207Ala
XM_011534514.1:c.619_621delinsGCG	XP_011532816.1:p.Thr207Ala
XM_011534515.1:c.148_150delinsGCG	XP_011532817.1:p.Thr50Ala
XR_941098.1:n.961_963delinsGCG
XR_941099.1:n.961_963delinsGCG
XR_941100.1:n.961_963delinsGCG
XM_011534515.2:c.148_150delinsGCG	XP_011532817.1:p.Thr50Ala
XM_017009339.2:c.619_621delinsGCG	XP_016864828.1:p.Thr207Ala
XM_024446019.1:c.619_621delinsGCG	XP_024301787.1:p.Thr207Ala
XM_024446020.1:c.619_621delinsGCG	XP_024301788.1:p.Thr207Ala
XM_024446021.1:c.619_621delinsGCG	XP_024301789.1:p.Thr207Ala
XM_024446022.1:c.619_621delinsGCG	XP_024301790.1:p.Thr207Ala
XM_024446023.1:c.619_621delinsGCG	XP_024301791.1:p.Thr207Ala
XM_024446024.1:c.619_621delinsGCG	XP_024301792.1:p.Thr207Ala
NM_001173393.3:c.619_621delinsGCG MANE Select	NP_001166864.1:p.Thr207Ala
NM_001308156.2:c.619_621delinsGCG	NP_001295085.1:p.Thr207Ala