Canonical Allele Identifier: CA409848054

Gene: TMPRSS15

Linked Data

• MyVariant Identifiers: chr21:g.19653462C>A (hg19) ; chr21:g.18281145C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281145C>A , CM000683.2:g.18281145C>A	GRCh38
NC_000021.8:g.19653462C>A , CM000683.1:g.19653462C>A	GRCh37
NC_000021.7:g.18575333C>A	NCBI36
NG_012207.1:g.127509G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2563G>T MANE Select	ENSP00000284885.3:p.Val855Phe
ENST00000284885.7:c.2563G>T	ENSP00000284885.3:p.Val855Phe
NM_002772.2:c.2563G>T	NP_002763.2:p.Val855Phe
XM_011529654.1:c.2698G>T	XP_011527956.1:p.Val900Phe
XM_011529655.1:c.2698G>T	XP_011527957.1:p.Val900Phe
XM_011529656.1:c.2698G>T	XP_011527958.1:p.Val900Phe
XM_011529657.1:c.2653G>T	XP_011527959.1:p.Val885Phe
XM_011529658.1:c.2617G>T	XP_011527960.1:p.Val873Phe
XM_011529659.1:c.2608G>T	XP_011527961.1:p.Val870Phe
XM_011529654.2:c.2698G>T	XP_011527956.1:p.Val900Phe
XM_011529656.2:c.2698G>T	XP_011527958.1:p.Val900Phe
XM_011529657.2:c.2653G>T	XP_011527959.1:p.Val885Phe
XM_011529658.2:c.2617G>T	XP_011527960.1:p.Val873Phe
NM_002772.3:c.2563G>T MANE Select	NP_002763.3:p.Val855Phe