Canonical Allele Identifier: CA2656484543

Gene: TMPRSS6

Linked Data

• gnomAD v4: 22-37075007-A-ACACACACAC

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37075008_37075016dup , CM000684.2:g.37075008_37075016dup	GRCh38
NC_000022.10:g.37471048_37471056dup , CM000684.1:g.37471048_37471056dup	GRCh37
NC_000022.9:g.35800994_35801002dup	NCBI36
NG_012856.2:g.39548_39556dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346753.9:c.1342+119_1342+127dup	ENSP00000334962.6:n.1342+119_1342+127dup
ENST00000406725.6:c.1342+119_1342+127dup	ENSP00000385453.1:n.1342+119_1342+127dup
ENST00000406856.7:c.1342+119_1342+127dup	ENSP00000384964.1:n.1342+119_1342+127dup
ENST00000676104.1:c.1342+119_1342+127dup MANE Select	ENSP00000501573.1:n.1342+119_1342+127dup
ENST00000346753.7:c.1369+119_1369+127dup	ENSP00000334962.5:n.1369+119_1369+127dup
ENST00000381792.6:c.1342+119_1342+127dup	ENSP00000371211.2:n.1342+119_1342+127dup
ENST00000406725.5:c.1342+119_1342+127dup	ENSP00000385453.1:n.1342+119_1342+127dup
ENST00000406856.5:c.1342+119_1342+127dup	ENSP00000384964.1:n.1342+119_1342+127dup
NM_001289000.1:c.1342+119_1342+127dup	NP_001275929.1:n.1342+119_1342+127dup
NM_001289001.1:c.1342+119_1342+127dup	NP_001275930.1:n.1342+119_1342+127dup
NM_153609.3:c.1369+119_1369+127dup	NP_705837.1:n.1369+119_1369+127dup
XM_006724162.1:c.1342+119_1342+127dup	XP_006724225.1:n.1342+119_1342+127dup
XM_006724163.2:c.1342+119_1342+127dup	XP_006724226.1:n.1342+119_1342+127dup
XM_011529987.1:c.1342+119_1342+127dup	XP_011528289.1:n.1342+119_1342+127dup
XM_011529988.1:c.1342+119_1342+127dup	XP_011528290.1:n.1342+119_1342+127dup
XM_011529989.1:c.910+119_910+127dup	XP_011528291.1:n.910+119_910+127dup
XM_011529989.2:c.910+119_910+127dup	XP_011528291.1:n.910+119_910+127dup
XM_024452167.1:c.1342+119_1342+127dup	XP_024307935.1:n.1342+119_1342+127dup
XM_024452168.1:c.1342+119_1342+127dup	XP_024307936.1:n.1342+119_1342+127dup
XM_024452169.1:c.1342+119_1342+127dup	XP_024307937.1:n.1342+119_1342+127dup
XM_024452170.1:c.1342+119_1342+127dup	XP_024307938.1:n.1342+119_1342+127dup
XM_024452171.1:c.1342+119_1342+127dup	XP_024307939.1:n.1342+119_1342+127dup
NM_001289000.2:c.1342+119_1342+127dup	NP_001275929.1:n.1342+119_1342+127dup
NM_001289001.2:c.1342+119_1342+127dup	NP_001275930.1:n.1342+119_1342+127dup
NM_001374504.1:c.1342+119_1342+127dup MANE Select	NP_001361433.1:n.1342+119_1342+127dup
NM_153609.4:c.1342+119_1342+127dup	NP_705837.2:n.1342+119_1342+127dup