Canonical Allele Identifier: CA2404171364

Gene: TMPRSS6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37075342_37075345delinsACAG , CM000684.2:g.37075342_37075345delinsACAG	GRCh38
NC_000022.10:g.37471382_37471385delinsACAG , CM000684.1:g.37471382_37471385delinsACAG	GRCh37
NC_000022.9:g.35801328_35801331delinsACAG	NCBI36
NG_012856.2:g.39219_39222delinsCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346753.9:c.1197-65_1197-62delinsCTGT	ENSP00000334962.6:n.1197-65_1197-62delinsCTGT
ENST00000406725.6:c.1197-65_1197-62delinsCTGT	ENSP00000385453.1:n.1197-65_1197-62delinsCTGT
ENST00000406856.7:c.1197-65_1197-62delinsCTGT	ENSP00000384964.1:n.1197-65_1197-62delinsCTGT
ENST00000676104.1:c.1197-65_1197-62delinsCTGT MANE Select	ENSP00000501573.1:n.1197-65_1197-62delinsCTGT
ENST00000346753.7:c.1224-65_1224-62delinsCTGT	ENSP00000334962.5:n.1224-65_1224-62delinsCTGT
ENST00000381792.6:c.1197-65_1197-62delinsCTGT	ENSP00000371211.2:n.1197-65_1197-62delinsCTGT
ENST00000406725.5:c.1197-65_1197-62delinsCTGT	ENSP00000385453.1:n.1197-65_1197-62delinsCTGT
ENST00000406856.5:c.1197-65_1197-62delinsCTGT	ENSP00000384964.1:n.1197-65_1197-62delinsCTGT
NM_001289000.1:c.1197-65_1197-62delinsCTGT	NP_001275929.1:n.1197-65_1197-62delinsCTGT
NM_001289001.1:c.1197-65_1197-62delinsCTGT	NP_001275930.1:n.1197-65_1197-62delinsCTGT
NM_153609.3:c.1224-65_1224-62delinsCTGT	NP_705837.1:n.1224-65_1224-62delinsCTGT
XM_006724162.1:c.1197-65_1197-62delinsCTGT	XP_006724225.1:n.1197-65_1197-62delinsCTGT
XM_006724163.2:c.1197-65_1197-62delinsCTGT	XP_006724226.1:n.1197-65_1197-62delinsCTGT
XM_011529987.1:c.1197-65_1197-62delinsCTGT	XP_011528289.1:n.1197-65_1197-62delinsCTGT
XM_011529988.1:c.1197-65_1197-62delinsCTGT	XP_011528290.1:n.1197-65_1197-62delinsCTGT
XM_011529989.1:c.765-65_765-62delinsCTGT	XP_011528291.1:n.765-65_765-62delinsCTGT
XM_011529989.2:c.765-65_765-62delinsCTGT	XP_011528291.1:n.765-65_765-62delinsCTGT
XM_024452167.1:c.1197-65_1197-62delinsCTGT	XP_024307935.1:n.1197-65_1197-62delinsCTGT
XM_024452168.1:c.1197-65_1197-62delinsCTGT	XP_024307936.1:n.1197-65_1197-62delinsCTGT
XM_024452169.1:c.1197-65_1197-62delinsCTGT	XP_024307937.1:n.1197-65_1197-62delinsCTGT
XM_024452170.1:c.1197-65_1197-62delinsCTGT	XP_024307938.1:n.1197-65_1197-62delinsCTGT
XM_024452171.1:c.1197-65_1197-62delinsCTGT	XP_024307939.1:n.1197-65_1197-62delinsCTGT
NM_001289000.2:c.1197-65_1197-62delinsCTGT	NP_001275929.1:n.1197-65_1197-62delinsCTGT
NM_001289001.2:c.1197-65_1197-62delinsCTGT	NP_001275930.1:n.1197-65_1197-62delinsCTGT
NM_001374504.1:c.1197-65_1197-62delinsCTGT MANE Select	NP_001361433.1:n.1197-65_1197-62delinsCTGT
NM_153609.4:c.1197-65_1197-62delinsCTGT	NP_705837.2:n.1197-65_1197-62delinsCTGT