Canonical Allele Identifier: CA409848050

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs527832914
• gnomAD v2: 21-19653459-G-A
• MyVariant Identifiers: chr21:g.19653459G>A (hg19) ; chr21:g.18281142G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281142G>A , CM000683.2:g.18281142G>A	GRCh38
NC_000021.8:g.19653459G>A , CM000683.1:g.19653459G>A	GRCh37
NC_000021.7:g.18575330G>A	NCBI36
NG_012207.1:g.127512C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2566C>T MANE Select	ENSP00000284885.3:p.Pro856Ser
ENST00000284885.7:c.2566C>T	ENSP00000284885.3:p.Pro856Ser
NM_002772.2:c.2566C>T	NP_002763.2:p.Pro856Ser
XM_011529654.1:c.2701C>T	XP_011527956.1:p.Pro901Ser
XM_011529655.1:c.2701C>T	XP_011527957.1:p.Pro901Ser
XM_011529656.1:c.2701C>T	XP_011527958.1:p.Pro901Ser
XM_011529657.1:c.2656C>T	XP_011527959.1:p.Pro886Ser
XM_011529658.1:c.2620C>T	XP_011527960.1:p.Pro874Ser
XM_011529659.1:c.2611C>T	XP_011527961.1:p.Pro871Ser
XM_011529654.2:c.2701C>T	XP_011527956.1:p.Pro901Ser
XM_011529656.2:c.2701C>T	XP_011527958.1:p.Pro901Ser
XM_011529657.2:c.2656C>T	XP_011527959.1:p.Pro886Ser
XM_011529658.2:c.2620C>T	XP_011527960.1:p.Pro874Ser
NM_002772.3:c.2566C>T MANE Select	NP_002763.3:p.Pro856Ser