Canonical Allele Identifier: CA409848125

Gene: TMPRSS15

Linked Data

• gnomAD v4: 21-18281178-G-A
• MyVariant Identifiers: chr21:g.19653495G>A (hg19) ; chr21:g.18281178G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281178G>A , CM000683.2:g.18281178G>A	GRCh38
NC_000021.8:g.19653495G>A , CM000683.1:g.19653495G>A	GRCh37
NC_000021.7:g.18575366G>A	NCBI36
NG_012207.1:g.127476C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2530C>T MANE Select	ENSP00000284885.3:p.His844Tyr
ENST00000284885.7:c.2530C>T	ENSP00000284885.3:p.His844Tyr
NM_002772.2:c.2530C>T	NP_002763.2:p.His844Tyr
XM_011529654.1:c.2665C>T	XP_011527956.1:p.His889Tyr
XM_011529655.1:c.2665C>T	XP_011527957.1:p.His889Tyr
XM_011529656.1:c.2665C>T	XP_011527958.1:p.His889Tyr
XM_011529657.1:c.2620C>T	XP_011527959.1:p.His874Tyr
XM_011529658.1:c.2584C>T	XP_011527960.1:p.His862Tyr
XM_011529659.1:c.2575C>T	XP_011527961.1:p.His859Tyr
XM_011529654.2:c.2665C>T	XP_011527956.1:p.His889Tyr
XM_011529656.2:c.2665C>T	XP_011527958.1:p.His889Tyr
XM_011529657.2:c.2620C>T	XP_011527959.1:p.His874Tyr
XM_011529658.2:c.2584C>T	XP_011527960.1:p.His862Tyr
NM_002772.3:c.2530C>T MANE Select	NP_002763.3:p.His844Tyr