Canonical Allele Identifier: CA2613948607

Gene: SCGB1A1

Linked Data

• gnomAD v4: 11-62419089-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62419090del , CM000673.2:g.62419090del	GRCh38
NC_000011.9:g.62186562del , CM000673.1:g.62186562del	GRCh37
NC_000011.8:g.61943138del	NCBI36
NG_021331.1:g.5056del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278282.3:c.-6del MANE Select	ENSP00000278282.2:n.-6del
ENST00000278282.2:c.-6del	ENSP00000278282.2:n.-6del
ENST00000534397.5:c.-51+2453del	ENSP00000432866.1:n.-51+2453del
NM_003357.4:c.-6del	NP_003348.1:n.-6del
XR_950170.1:n.378-2240del
XR_950171.1:n.234-2240del
XR_950172.1:n.234-2240del
XR_950173.1:n.234-2240del
XR_950174.1:n.234-2240del
XR_001748247.1:n.348-2240del
XR_001748248.1:n.453-2240del
XR_001748249.1:n.459-2240del
XR_001748250.1:n.455-2240del
XR_001748252.1:n.460-2240del
XR_001748253.1:n.180-2240del
XR_001748254.1:n.461-2240del
XR_002957250.1:n.451-2240del
NM_003357.5:c.-6del MANE Select	NP_003348.1:n.-6del