Canonical Allele Identifier: CA409847847

Gene: TMPRSS15

Linked Data

• MyVariant Identifiers: chr21:g.19653368A>G (hg19) ; chr21:g.18281051A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281051A>G , CM000683.2:g.18281051A>G	GRCh38
NC_000021.8:g.19653368A>G , CM000683.1:g.19653368A>G	GRCh37
NC_000021.7:g.18575239A>G	NCBI36
NG_012207.1:g.127603T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2657T>C MANE Select	ENSP00000284885.3:p.Val886Ala
ENST00000284885.7:c.2657T>C	ENSP00000284885.3:p.Val886Ala
NM_002772.2:c.2657T>C	NP_002763.2:p.Val886Ala
XM_011529654.1:c.2792T>C	XP_011527956.1:p.Val931Ala
XM_011529655.1:c.2792T>C	XP_011527957.1:p.Val931Ala
XM_011529656.1:c.2792T>C	XP_011527958.1:p.Val931Ala
XM_011529657.1:c.2747T>C	XP_011527959.1:p.Val916Ala
XM_011529658.1:c.2711T>C	XP_011527960.1:p.Val904Ala
XM_011529659.1:c.2702T>C	XP_011527961.1:p.Val901Ala
XM_011529654.2:c.2792T>C	XP_011527956.1:p.Val931Ala
XM_011529656.2:c.2792T>C	XP_011527958.1:p.Val931Ala
XM_011529657.2:c.2747T>C	XP_011527959.1:p.Val916Ala
XM_011529658.2:c.2711T>C	XP_011527960.1:p.Val904Ala
NM_002772.3:c.2657T>C MANE Select	NP_002763.3:p.Val886Ala