Canonical Allele Identifier: CA409848137

Gene: TMPRSS15

Linked Data

• gnomAD v4: 21-18281184-C-G
• MyVariant Identifiers: chr21:g.19653501C>G (hg19) ; chr21:g.18281184C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281184C>G , CM000683.2:g.18281184C>G	GRCh38
NC_000021.8:g.19653501C>G , CM000683.1:g.19653501C>G	GRCh37
NC_000021.7:g.18575372C>G	NCBI36
NG_012207.1:g.127470G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2524G>C MANE Select	ENSP00000284885.3:p.Gly842Arg
ENST00000284885.7:c.2524G>C	ENSP00000284885.3:p.Gly842Arg
NM_002772.2:c.2524G>C	NP_002763.2:p.Gly842Arg
XM_011529654.1:c.2659G>C	XP_011527956.1:p.Gly887Arg
XM_011529655.1:c.2659G>C	XP_011527957.1:p.Gly887Arg
XM_011529656.1:c.2659G>C	XP_011527958.1:p.Gly887Arg
XM_011529657.1:c.2614G>C	XP_011527959.1:p.Gly872Arg
XM_011529658.1:c.2578G>C	XP_011527960.1:p.Gly860Arg
XM_011529659.1:c.2569G>C	XP_011527961.1:p.Gly857Arg
XM_011529654.2:c.2659G>C	XP_011527956.1:p.Gly887Arg
XM_011529656.2:c.2659G>C	XP_011527958.1:p.Gly887Arg
XM_011529657.2:c.2614G>C	XP_011527959.1:p.Gly872Arg
XM_011529658.2:c.2578G>C	XP_011527960.1:p.Gly860Arg
NM_002772.3:c.2524G>C MANE Select	NP_002763.3:p.Gly842Arg