Canonical Allele Identifier: CA511459136

Gene: TMPRSS15

Linked Data

• MyVariant Identifiers: chr21:g.19653457A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281140A>C , CM000683.2:g.18281140A>C	GRCh38
NC_000021.8:g.19653457A>C , CM000683.1:g.19653457A>C	GRCh37
NC_000021.7:g.18575328A>C	NCBI36
NG_012207.1:g.127514T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2568T>G MANE Select	ENSP00000284885.3:p.Pro856=
ENST00000284885.7:c.2568T>G	ENSP00000284885.3:p.Pro856=
NM_002772.2:c.2568T>G	NP_002763.2:p.Pro856=
XM_011529654.1:c.2703T>G	XP_011527956.1:p.Pro901=
XM_011529655.1:c.2703T>G	XP_011527957.1:p.Pro901=
XM_011529656.1:c.2703T>G	XP_011527958.1:p.Pro901=
XM_011529657.1:c.2658T>G	XP_011527959.1:p.Pro886=
XM_011529658.1:c.2622T>G	XP_011527960.1:p.Pro874=
XM_011529659.1:c.2613T>G	XP_011527961.1:p.Pro871=
XM_011529654.2:c.2703T>G	XP_011527956.1:p.Pro901=
XM_011529656.2:c.2703T>G	XP_011527958.1:p.Pro901=
XM_011529657.2:c.2658T>G	XP_011527959.1:p.Pro886=
XM_011529658.2:c.2622T>G	XP_011527960.1:p.Pro874=
NM_002772.3:c.2568T>G MANE Select	NP_002763.3:p.Pro856=