Canonical Allele Identifier: CA511459100

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs1474437984
• gnomAD v2: 21-19653382-A-G
• gnomAD v4: 21-18281065-A-G
• MyVariant Identifiers: chr21:g.19653382A>G (hg19) ; chr21:g.18281065A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281065A>G , CM000683.2:g.18281065A>G	GRCh38
NC_000021.8:g.19653382A>G , CM000683.1:g.19653382A>G	GRCh37
NC_000021.7:g.18575253A>G	NCBI36
NG_012207.1:g.127589T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2643T>C MANE Select	ENSP00000284885.3:p.His881=
ENST00000284885.7:c.2643T>C	ENSP00000284885.3:p.His881=
NM_002772.2:c.2643T>C	NP_002763.2:p.His881=
XM_011529654.1:c.2778T>C	XP_011527956.1:p.His926=
XM_011529655.1:c.2778T>C	XP_011527957.1:p.His926=
XM_011529656.1:c.2778T>C	XP_011527958.1:p.His926=
XM_011529657.1:c.2733T>C	XP_011527959.1:p.His911=
XM_011529658.1:c.2697T>C	XP_011527960.1:p.His899=
XM_011529659.1:c.2688T>C	XP_011527961.1:p.His896=
XM_011529654.2:c.2778T>C	XP_011527956.1:p.His926=
XM_011529656.2:c.2778T>C	XP_011527958.1:p.His926=
XM_011529657.2:c.2733T>C	XP_011527959.1:p.His911=
XM_011529658.2:c.2697T>C	XP_011527960.1:p.His899=
NM_002772.3:c.2643T>C MANE Select	NP_002763.3:p.His881=