Canonical Allele Identifier: CA511459178

Gene: TMPRSS15

Linked Data

• MyVariant Identifiers: chr21:g.19653508T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281191T>G , CM000683.2:g.18281191T>G	GRCh38
NC_000021.8:g.19653508T>G , CM000683.1:g.19653508T>G	GRCh37
NC_000021.7:g.18575379T>G	NCBI36
NG_012207.1:g.127463A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2517A>C MANE Select	ENSP00000284885.3:p.Ala839=
ENST00000284885.7:c.2517A>C	ENSP00000284885.3:p.Ala839=
NM_002772.2:c.2517A>C	NP_002763.2:p.Ala839=
XM_011529654.1:c.2652A>C	XP_011527956.1:p.Ala884=
XM_011529655.1:c.2652A>C	XP_011527957.1:p.Ala884=
XM_011529656.1:c.2652A>C	XP_011527958.1:p.Ala884=
XM_011529657.1:c.2607A>C	XP_011527959.1:p.Ala869=
XM_011529658.1:c.2571A>C	XP_011527960.1:p.Ala857=
XM_011529659.1:c.2562A>C	XP_011527961.1:p.Ala854=
XM_011529654.2:c.2652A>C	XP_011527956.1:p.Ala884=
XM_011529656.2:c.2652A>C	XP_011527958.1:p.Ala884=
XM_011529657.2:c.2607A>C	XP_011527959.1:p.Ala869=
XM_011529658.2:c.2571A>C	XP_011527960.1:p.Ala857=
NM_002772.3:c.2517A>C MANE Select	NP_002763.3:p.Ala839=