Canonical Allele Identifier: CA645526988

Gene: CD207

Linked Data

• COSMIC: COSM6092024

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831738_70831739delinsAA , CM000664.2:g.70831738_70831739delinsAA	GRCh38
NC_000002.11:g.71058869_71058870delinsAA , CM000664.1:g.71058869_71058870delinsAA	GRCh37
NC_000002.10:g.70912377_70912378delinsAA	NCBI36
NG_033914.1:g.9085_9086delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.798_799delinsTT MANE Select	ENSP00000386378.3:p.Trp266_Val267delinsCysLeu
ENST00000410009.4:c.798_799delinsTT	ENSP00000386378.3:p.Trp266_Val267delinsCysLeu
NM_015717.4:c.798_799delinsTT	NP_056532.4:p.Trp266_Val267delinsCysLeu
XM_011532874.1:c.798_799delinsTT	XP_011531176.1:p.Trp266_Val267delinsCysLeu
XM_011532875.1:c.798_799delinsTT	XP_011531177.1:p.Trp266_Val267delinsCysLeu
XM_011532876.1:c.798_799delinsTT	XP_011531178.1:p.Trp266_Val267delinsCysLeu
XM_011532875.2:c.798_799delinsTT	XP_011531177.1:p.Trp266_Val267delinsCysLeu
XM_011532876.2:c.798_799delinsTT	XP_011531178.1:p.Trp266_Val267delinsCysLeu
NM_015717.5:c.798_799delinsTT MANE Select	NP_056532.4:p.Trp266_Val267delinsCysLeu