Canonical Allele Identifier: CA409847944

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs1339214041
• gnomAD v2: 21-19653407-T-G
• gnomAD v4: 21-18281090-T-G
• MyVariant Identifiers: chr21:g.19653407T>G (hg19) ; chr21:g.18281090T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281090T>G , CM000683.2:g.18281090T>G	GRCh38
NC_000021.8:g.19653407T>G , CM000683.1:g.19653407T>G	GRCh37
NC_000021.7:g.18575278T>G	NCBI36
NG_012207.1:g.127564A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2618A>C MANE Select	ENSP00000284885.3:p.Lys873Thr
ENST00000284885.7:c.2618A>C	ENSP00000284885.3:p.Lys873Thr
NM_002772.2:c.2618A>C	NP_002763.2:p.Lys873Thr
XM_011529654.1:c.2753A>C	XP_011527956.1:p.Lys918Thr
XM_011529655.1:c.2753A>C	XP_011527957.1:p.Lys918Thr
XM_011529656.1:c.2753A>C	XP_011527958.1:p.Lys918Thr
XM_011529657.1:c.2708A>C	XP_011527959.1:p.Lys903Thr
XM_011529658.1:c.2672A>C	XP_011527960.1:p.Lys891Thr
XM_011529659.1:c.2663A>C	XP_011527961.1:p.Lys888Thr
XM_011529654.2:c.2753A>C	XP_011527956.1:p.Lys918Thr
XM_011529656.2:c.2753A>C	XP_011527958.1:p.Lys918Thr
XM_011529657.2:c.2708A>C	XP_011527959.1:p.Lys903Thr
XM_011529658.2:c.2672A>C	XP_011527960.1:p.Lys891Thr
NM_002772.3:c.2618A>C MANE Select	NP_002763.3:p.Lys873Thr