Canonical Allele Identifier: CA2654083062

Gene: TMPRSS15

Linked Data

• gnomAD v4: 21-18280978-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18280978G>T , CM000683.2:g.18280978G>T	GRCh38
NC_000021.8:g.19653295G>T , CM000683.1:g.19653295G>T	GRCh37
NC_000021.7:g.18575166G>T	NCBI36
NG_012207.1:g.127676C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2668+62C>A MANE Select	ENSP00000284885.3:n.2668+62C>A
ENST00000284885.7:c.2668+62C>A	ENSP00000284885.3:n.2668+62C>A
NM_002772.2:c.2668+62C>A	NP_002763.2:n.2668+62C>A
XM_011529654.1:c.2803+62C>A	XP_011527956.1:n.2803+62C>A
XM_011529655.1:c.2803+62C>A	XP_011527957.1:n.2803+62C>A
XM_011529656.1:c.2803+62C>A	XP_011527958.1:n.2803+62C>A
XM_011529657.1:c.2758+62C>A	XP_011527959.1:n.2758+62C>A
XM_011529658.1:c.2722+62C>A	XP_011527960.1:n.2722+62C>A
XM_011529659.1:c.2713+62C>A	XP_011527961.1:n.2713+62C>A
XM_011529654.2:c.2803+62C>A	XP_011527956.1:n.2803+62C>A
XM_011529656.2:c.2803+62C>A	XP_011527958.1:n.2803+62C>A
XM_011529657.2:c.2758+62C>A	XP_011527959.1:n.2758+62C>A
XM_011529658.2:c.2722+62C>A	XP_011527960.1:n.2722+62C>A
NM_002772.3:c.2668+62C>A MANE Select	NP_002763.3:n.2668+62C>A