Canonical Allele Identifier: CA6043381

Gene: SCGB1A1

Linked Data

• dbSNP Id: rs778619687
• ExAC: 11:62186562 TCCA / T
• gnomAD v2: 11-62186562-TCCA-T
• gnomAD v3: 11-62419090-TCCA-T
• gnomAD v4: 11-62419090-TCCA-T
• MyVariant Identifiers: chr11:g.62186563_62186565del (hg19) ; chr11:g.62419091_62419093del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62419094_62419096del , CM000673.2:g.62419094_62419096del	GRCh38
NC_000011.9:g.62186566_62186568del , CM000673.1:g.62186566_62186568del	GRCh37
NC_000011.8:g.61943142_61943144del	NCBI36
NG_021331.1:g.5060_5062del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278282.3:c.-2_1del MANE Select	ENSP00000278282.2:n.-2_1del
ENST00000278282.2:c.-2_1del	ENSP00000278282.2:n.-2_1del
ENST00000534397.5:c.-51+2457_-51+2459del	ENSP00000432866.1:n.-51+2457_-51+2459del
NM_003357.4:c.-2_1del	NP_003348.1:n.-2_1del
XR_950170.1:n.378-2243_378-2241del
XR_950171.1:n.234-2243_234-2241del
XR_950172.1:n.234-2243_234-2241del
XR_950173.1:n.234-2243_234-2241del
XR_950174.1:n.234-2243_234-2241del
XR_001748247.1:n.348-2243_348-2241del
XR_001748248.1:n.453-2243_453-2241del
XR_001748249.1:n.459-2243_459-2241del
XR_001748250.1:n.455-2243_455-2241del
XR_001748252.1:n.460-2243_460-2241del
XR_001748253.1:n.180-2243_180-2241del
XR_001748254.1:n.461-2243_461-2241del
XR_002957250.1:n.451-2243_451-2241del
NM_003357.5:c.-2_1del MANE Select	NP_003348.1:n.-2_1del