Canonical Allele Identifier: CA1259751372

Gene: CD207

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70832034_70832035delinsCA , CM000664.2:g.70832034_70832035delinsCA	GRCh38
NC_000002.11:g.71059165_71059166delinsCA , CM000664.1:g.71059165_71059166delinsCA	GRCh37
NC_000002.10:g.70912673_70912674delinsCA	NCBI36
NG_033914.1:g.8789_8790delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.718-216_718-215delinsTG MANE Select	ENSP00000386378.3:n.718-216_718-215delinsTG
ENST00000410009.4:c.718-216_718-215delinsTG	ENSP00000386378.3:n.718-216_718-215delinsTG
NM_015717.4:c.718-216_718-215delinsTG	NP_056532.4:n.718-216_718-215delinsTG
XM_011532874.1:c.718-216_718-215delinsTG	XP_011531176.1:n.718-216_718-215delinsTG
XM_011532875.1:c.718-216_718-215delinsTG	XP_011531177.1:n.718-216_718-215delinsTG
XM_011532876.1:c.718-216_718-215delinsTG	XP_011531178.1:n.718-216_718-215delinsTG
XM_011532875.2:c.718-216_718-215delinsTG	XP_011531177.1:n.718-216_718-215delinsTG
XM_011532876.2:c.718-216_718-215delinsTG	XP_011531178.1:n.718-216_718-215delinsTG
NM_015717.5:c.718-216_718-215delinsTG MANE Select	NP_056532.4:n.718-216_718-215delinsTG