Canonical Allele Identifier: CA1259751167

Gene: CD207

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831618_70831619delinsTG , CM000664.2:g.70831618_70831619delinsTG	GRCh38
NC_000002.11:g.71058749_71058750delinsTG , CM000664.1:g.71058749_71058750delinsTG	GRCh37
NC_000002.10:g.70912257_70912258delinsTG	NCBI36
NG_033914.1:g.9205_9206delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.836+82_836+83delinsCA MANE Select	ENSP00000386378.3:n.836+82_836+83delinsCA
ENST00000410009.4:c.836+82_836+83delinsCA	ENSP00000386378.3:n.836+82_836+83delinsCA
NM_015717.4:c.836+82_836+83delinsCA	NP_056532.4:n.836+82_836+83delinsCA
XM_011532874.1:c.836+82_836+83delinsCA	XP_011531176.1:n.836+82_836+83delinsCA
XM_011532875.1:c.836+82_836+83delinsCA	XP_011531177.1:n.836+82_836+83delinsCA
XM_011532876.1:c.836+82_836+83delinsCA	XP_011531178.1:n.836+82_836+83delinsCA
XM_011532875.2:c.836+82_836+83delinsCA	XP_011531177.1:n.836+82_836+83delinsCA
XM_011532876.2:c.836+82_836+83delinsCA	XP_011531178.1:n.836+82_836+83delinsCA
NM_015717.5:c.836+82_836+83delinsCA MANE Select	NP_056532.4:n.836+82_836+83delinsCA