Canonical Allele Identifier: CA511459092

Gene: TMPRSS15

Linked Data

• MyVariant Identifiers: chr21:g.19653367C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281050C>G , CM000683.2:g.18281050C>G	GRCh38
NC_000021.8:g.19653367C>G , CM000683.1:g.19653367C>G	GRCh37
NC_000021.7:g.18575238C>G	NCBI36
NG_012207.1:g.127604G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2658G>C MANE Select	ENSP00000284885.3:p.Val886=
ENST00000284885.7:c.2658G>C	ENSP00000284885.3:p.Val886=
NM_002772.2:c.2658G>C	NP_002763.2:p.Val886=
XM_011529654.1:c.2793G>C	XP_011527956.1:p.Val931=
XM_011529655.1:c.2793G>C	XP_011527957.1:p.Val931=
XM_011529656.1:c.2793G>C	XP_011527958.1:p.Val931=
XM_011529657.1:c.2748G>C	XP_011527959.1:p.Val916=
XM_011529658.1:c.2712G>C	XP_011527960.1:p.Val904=
XM_011529659.1:c.2703G>C	XP_011527961.1:p.Val901=
XM_011529654.2:c.2793G>C	XP_011527956.1:p.Val931=
XM_011529656.2:c.2793G>C	XP_011527958.1:p.Val931=
XM_011529657.2:c.2748G>C	XP_011527959.1:p.Val916=
XM_011529658.2:c.2712G>C	XP_011527960.1:p.Val904=
NM_002772.3:c.2658G>C MANE Select	NP_002763.3:p.Val886=