Canonical Allele Identifier: CA347179589

Gene: CD207

Linked Data

• COSMIC: COSM1615065
• MyVariant Identifiers: chr2:g.71058938T>A (hg19) ; chr2:g.70831807T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831807T>A , CM000664.2:g.70831807T>A	GRCh38
NC_000002.11:g.71058938T>A , CM000664.1:g.71058938T>A	GRCh37
NC_000002.10:g.70912446T>A	NCBI36
NG_033914.1:g.9017A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.730A>T MANE Select	ENSP00000386378.3:p.Lys244Ter
ENST00000410009.4:c.730A>T	ENSP00000386378.3:p.Lys244Ter
NM_015717.4:c.730A>T	NP_056532.4:p.Lys244Ter
XM_011532874.1:c.730A>T	XP_011531176.1:p.Lys244Ter
XM_011532875.1:c.730A>T	XP_011531177.1:p.Lys244Ter
XM_011532876.1:c.730A>T	XP_011531178.1:p.Lys244Ter
XM_011532875.2:c.730A>T	XP_011531177.1:p.Lys244Ter
XM_011532876.2:c.730A>T	XP_011531178.1:p.Lys244Ter
NM_015717.5:c.730A>T MANE Select	NP_056532.4:p.Lys244Ter