Canonical Allele Identifier: CA2613948385
Gene: SCGB1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62418915_62418916insAAGCCAC , CM000673.2:g.62418915_62418916insAAGCCAC GRCh38
NC_000011.9:g.62186387_62186388insAAGCCAC , CM000673.1:g.62186387_62186388insAAGCCAC GRCh37
NC_000011.8:g.61942963_61942964insAAGCCAC NCBI36
NG_021331.1:g.4881_4882insAAGCCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000534397.5:c.-51+2278_-51+2279insAAGCCAC ENSP00000432866.1:n.-51+2278_-51+2279insAAGCCAC
XR_950170.1:n.378-2065_378-2064insTGGCTTG
XR_950171.1:n.234-2065_234-2064insTGGCTTG
XR_950172.1:n.234-2065_234-2064insTGGCTTG
XR_950173.1:n.234-2065_234-2064insTGGCTTG
XR_950174.1:n.234-2065_234-2064insTGGCTTG
XR_001748247.1:n.348-2065_348-2064insTGGCTTG
XR_001748248.1:n.453-2065_453-2064insTGGCTTG
XR_001748249.1:n.459-2065_459-2064insTGGCTTG
XR_001748250.1:n.455-2065_455-2064insTGGCTTG
XR_001748252.1:n.460-2065_460-2064insTGGCTTG
XR_001748253.1:n.180-2065_180-2064insTGGCTTG
XR_001748254.1:n.461-2065_461-2064insTGGCTTG
XR_002957250.1:n.451-2065_451-2064insTGGCTTG