Canonical Allele Identifier: CA2613948583
Gene: SCGB1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62419077_62419078del , CM000673.2:g.62419077_62419078del GRCh38
NC_000011.9:g.62186549_62186550del , CM000673.1:g.62186549_62186550del GRCh37
NC_000011.8:g.61943125_61943126del NCBI36
NG_021331.1:g.5043_5044del

Transcript Alleles

HGVS Amino-acid change
ENST00000278282.3:c.-19_-18del MANE Select ENSP00000278282.2:n.-19_-18del
ENST00000278282.2:c.-19_-18del ENSP00000278282.2:n.-19_-18del
ENST00000534397.5:c.-51+2440_-51+2441del ENSP00000432866.1:n.-51+2440_-51+2441del
NM_003357.4:c.-19_-18del NP_003348.1:n.-19_-18del
XR_950170.1:n.378-2226_378-2225del
XR_950171.1:n.234-2226_234-2225del
XR_950172.1:n.234-2226_234-2225del
XR_950173.1:n.234-2226_234-2225del
XR_950174.1:n.234-2226_234-2225del
XR_001748247.1:n.348-2226_348-2225del
XR_001748248.1:n.453-2226_453-2225del
XR_001748249.1:n.459-2226_459-2225del
XR_001748250.1:n.455-2226_455-2225del
XR_001748252.1:n.460-2226_460-2225del
XR_001748253.1:n.180-2226_180-2225del
XR_001748254.1:n.461-2226_461-2225del
XR_002957250.1:n.451-2226_451-2225del
NM_003357.5:c.-19_-18del MANE Select NP_003348.1:n.-19_-18del