Canonical Allele Identifier: CA552162452

Gene: TMPRSS11A

Linked Data

• dbSNP Id: rs1344061695
• gnomAD v2: 4-68797877-GAACT-G
• gnomAD v3: 4-67932159-GAACT-G
• gnomAD v4: 4-67932159-GAACT-G
• MyVariant Identifiers: chr4:g.68797878_68797881del (hg19) ; chr4:g.67932160_67932163del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67932163_67932166del , CM000666.2:g.67932163_67932166del	GRCh38
NC_000004.11:g.68797881_68797884del , CM000666.1:g.68797881_68797884del	GRCh37
NC_000004.10:g.68480476_68480479del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508048.6:c.253-103_253-100del MANE Select	ENSP00000426911.2:n.253-103_253-100del
ENST00000334830.11:c.262-103_262-100del	ENSP00000334611.7:n.262-103_262-100del
ENST00000396188.3:c.253-103_253-100del	ENSP00000379491.3:n.253-103_253-100del
ENST00000508048.5:c.253-103_253-100del	ENSP00000426911.2:n.253-103_253-100del
ENST00000513536.5:c.193-103_193-100del	ENSP00000427621.1:n.193-103_193-100del
NM_001114387.1:c.253-103_253-100del	NP_001107859.1:n.253-103_253-100del
NM_182606.3:c.262-103_262-100del	NP_872412.3:n.262-103_262-100del
NM_001114387.2:c.253-103_253-100del MANE Select	NP_001107859.1:n.253-103_253-100del
NM_182606.4:c.262-103_262-100del	NP_872412.3:n.262-103_262-100del