Canonical Allele Identifier: CA9984175

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs368892564
• ExAC: 21:19685224 G / A
• gnomAD v2: 21-19685224-G-A
• gnomAD v3: 21-18312907-G-A
• gnomAD v4: 21-18312907-G-A
• MyVariant Identifiers: chr21:g.19685224G>A (hg19) ; chr21:g.18312907G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18312907G>A , CM000683.2:g.18312907G>A	GRCh38
NC_000021.8:g.19685224G>A , CM000683.1:g.19685224G>A	GRCh37
NC_000021.7:g.18607095G>A	NCBI36
NG_012207.1:g.95747C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2165+38C>T MANE Select	ENSP00000284885.3:n.2165+38C>T
ENST00000284885.7:c.2165+38C>T	ENSP00000284885.3:n.2165+38C>T
NM_002772.2:c.2165+38C>T	NP_002763.2:n.2165+38C>T
XM_011529654.1:c.2300+38C>T	XP_011527956.1:n.2300+38C>T
XM_011529655.1:c.2300+38C>T	XP_011527957.1:n.2300+38C>T
XM_011529656.1:c.2300+38C>T	XP_011527958.1:n.2300+38C>T
XM_011529657.1:c.2255+38C>T	XP_011527959.1:n.2255+38C>T
XM_011529658.1:c.2219+38C>T	XP_011527960.1:n.2219+38C>T
XM_011529659.1:c.2210+38C>T	XP_011527961.1:n.2210+38C>T
XM_011529654.2:c.2300+38C>T	XP_011527956.1:n.2300+38C>T
XM_011529656.2:c.2300+38C>T	XP_011527958.1:n.2300+38C>T
XM_011529657.2:c.2255+38C>T	XP_011527959.1:n.2255+38C>T
XM_011529658.2:c.2219+38C>T	XP_011527960.1:n.2219+38C>T
NM_002772.3:c.2165+38C>T MANE Select	NP_002763.3:n.2165+38C>T