Canonical Allele Identifier: CA2379736648

Gene: TMPRSS15

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281070_18281071delinsTC , CM000683.2:g.18281070_18281071delinsTC	GRCh38
NC_000021.8:g.19653387_19653388delinsTC , CM000683.1:g.19653387_19653388delinsTC	GRCh37
NC_000021.7:g.18575258_18575259delinsTC	NCBI36
NG_012207.1:g.127583_127584delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2637_2638delinsGA MANE Select	ENSP00000284885.3:p.Met879=
ENST00000284885.7:c.2637_2638delinsGA	ENSP00000284885.3:p.Met879=
NM_002772.2:c.2637_2638delinsGA	NP_002763.2:p.Met879=
XM_011529654.1:c.2772_2773delinsGA	XP_011527956.1:p.Met924=
XM_011529655.1:c.2772_2773delinsGA	XP_011527957.1:p.Met924=
XM_011529656.1:c.2772_2773delinsGA	XP_011527958.1:p.Met924=
XM_011529657.1:c.2727_2728delinsGA	XP_011527959.1:p.Met909=
XM_011529658.1:c.2691_2692delinsGA	XP_011527960.1:p.Met897=
XM_011529659.1:c.2682_2683delinsGA	XP_011527961.1:p.Met894=
XM_011529654.2:c.2772_2773delinsGA	XP_011527956.1:p.Met924=
XM_011529656.2:c.2772_2773delinsGA	XP_011527958.1:p.Met924=
XM_011529657.2:c.2727_2728delinsGA	XP_011527959.1:p.Met909=
XM_011529658.2:c.2691_2692delinsGA	XP_011527960.1:p.Met897=
NM_002772.3:c.2637_2638delinsGA MANE Select	NP_002763.3:p.Met879=