Canonical Allele Identifier: CA409848030

Gene: TMPRSS15

Linked Data

• MyVariant Identifiers: chr21:g.19653447C>G (hg19) ; chr21:g.18281130C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281130C>G , CM000683.2:g.18281130C>G	GRCh38
NC_000021.8:g.19653447C>G , CM000683.1:g.19653447C>G	GRCh37
NC_000021.7:g.18575318C>G	NCBI36
NG_012207.1:g.127524G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2578G>C MANE Select	ENSP00000284885.3:p.Asp860His
ENST00000284885.7:c.2578G>C	ENSP00000284885.3:p.Asp860His
NM_002772.2:c.2578G>C	NP_002763.2:p.Asp860His
XM_011529654.1:c.2713G>C	XP_011527956.1:p.Asp905His
XM_011529655.1:c.2713G>C	XP_011527957.1:p.Asp905His
XM_011529656.1:c.2713G>C	XP_011527958.1:p.Asp905His
XM_011529657.1:c.2668G>C	XP_011527959.1:p.Asp890His
XM_011529658.1:c.2632G>C	XP_011527960.1:p.Asp878His
XM_011529659.1:c.2623G>C	XP_011527961.1:p.Asp875His
XM_011529654.2:c.2713G>C	XP_011527956.1:p.Asp905His
XM_011529656.2:c.2713G>C	XP_011527958.1:p.Asp905His
XM_011529657.2:c.2668G>C	XP_011527959.1:p.Asp890His
XM_011529658.2:c.2632G>C	XP_011527960.1:p.Asp878His
NM_002772.3:c.2578G>C MANE Select	NP_002763.3:p.Asp860His