Canonical Allele Identifier: CA9983971

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs768845703
• ExAC: 21:19653312 TA / T
• gnomAD v2: 21-19653312-TA-T
• gnomAD v3: 21-18280995-TA-T
• gnomAD v4: 21-18280995-TA-T
• MyVariant Identifiers: chr21:g.19653313del (hg19) ; chr21:g.18280997del (hg38) ; chr21:g.18280996del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18280997del , CM000683.2:g.18280997del	GRCh38
NC_000021.8:g.19653314del , CM000683.1:g.19653314del	GRCh37
NC_000021.7:g.18575185del	NCBI36
NG_012207.1:g.127658del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2668+44del MANE Select	ENSP00000284885.3:n.2668+44del
ENST00000284885.7:c.2668+44del	ENSP00000284885.3:n.2668+44del
NM_002772.2:c.2668+44del	NP_002763.2:n.2668+44del
XM_011529654.1:c.2803+44del	XP_011527956.1:n.2803+44del
XM_011529655.1:c.2803+44del	XP_011527957.1:n.2803+44del
XM_011529656.1:c.2803+44del	XP_011527958.1:n.2803+44del
XM_011529657.1:c.2758+44del	XP_011527959.1:n.2758+44del
XM_011529658.1:c.2722+44del	XP_011527960.1:n.2722+44del
XM_011529659.1:c.2713+44del	XP_011527961.1:n.2713+44del
XM_011529654.2:c.2803+44del	XP_011527956.1:n.2803+44del
XM_011529656.2:c.2803+44del	XP_011527958.1:n.2803+44del
XM_011529657.2:c.2758+44del	XP_011527959.1:n.2758+44del
XM_011529658.2:c.2722+44del	XP_011527960.1:n.2722+44del
NM_002772.3:c.2668+44del MANE Select	NP_002763.3:n.2668+44del