Canonical Allele Identifier: CA9984005

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs146521830
• ExAC: 21:19653461 A / G
• gnomAD v2: 21-19653461-A-G
• gnomAD v3: 21-18281144-A-G
• gnomAD v4: 21-18281144-A-G
• MyVariant Identifiers: chr21:g.19653461A>G (hg19) ; chr21:g.18281144A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281144A>G , CM000683.2:g.18281144A>G	GRCh38
NC_000021.8:g.19653461A>G , CM000683.1:g.19653461A>G	GRCh37
NC_000021.7:g.18575332A>G	NCBI36
NG_012207.1:g.127510T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2564T>C MANE Select	ENSP00000284885.3:p.Val855Ala
ENST00000284885.7:c.2564T>C	ENSP00000284885.3:p.Val855Ala
NM_002772.2:c.2564T>C	NP_002763.2:p.Val855Ala
XM_011529654.1:c.2699T>C	XP_011527956.1:p.Val900Ala
XM_011529655.1:c.2699T>C	XP_011527957.1:p.Val900Ala
XM_011529656.1:c.2699T>C	XP_011527958.1:p.Val900Ala
XM_011529657.1:c.2654T>C	XP_011527959.1:p.Val885Ala
XM_011529658.1:c.2618T>C	XP_011527960.1:p.Val873Ala
XM_011529659.1:c.2609T>C	XP_011527961.1:p.Val870Ala
XM_011529654.2:c.2699T>C	XP_011527956.1:p.Val900Ala
XM_011529656.2:c.2699T>C	XP_011527958.1:p.Val900Ala
XM_011529657.2:c.2654T>C	XP_011527959.1:p.Val885Ala
XM_011529658.2:c.2618T>C	XP_011527960.1:p.Val873Ala
NM_002772.3:c.2564T>C MANE Select	NP_002763.3:p.Val855Ala