Canonical Allele Identifier: CA1259751229

Gene: CD207

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831728_70831729delinsGT , CM000664.2:g.70831728_70831729delinsGT	GRCh38
NC_000002.11:g.71058859_71058860delinsGT , CM000664.1:g.71058859_71058860delinsGT	GRCh37
NC_000002.10:g.70912367_70912368delinsGT	NCBI36
NG_033914.1:g.9095_9096delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.808_809delinsAC MANE Select	ENSP00000386378.3:p.Thr270=
ENST00000410009.4:c.808_809delinsAC	ENSP00000386378.3:p.Thr270=
NM_015717.4:c.808_809delinsAC	NP_056532.4:p.Thr270=
XM_011532874.1:c.808_809delinsAC	XP_011531176.1:p.Thr270=
XM_011532875.1:c.808_809delinsAC	XP_011531177.1:p.Thr270=
XM_011532876.1:c.808_809delinsAC	XP_011531178.1:p.Thr270=
XM_011532875.2:c.808_809delinsAC	XP_011531177.1:p.Thr270=
XM_011532876.2:c.808_809delinsAC	XP_011531178.1:p.Thr270=
NM_015717.5:c.808_809delinsAC MANE Select	NP_056532.4:p.Thr270=