Canonical Allele Identifier: CA1977752096

Gene: SCGB1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62419070G= , CM000673.2:g.62419070G=	GRCh38
NC_000011.9:g.62186542G= , CM000673.1:g.62186542G=	GRCh37
NC_000011.8:g.61943118G=	NCBI36
NG_021331.1:g.5036G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000278282.3:c.-26G= MANE Select	ENSP00000278282.2:n.-26G=
ENST00000278282.2:c.-26G=	ENSP00000278282.2:n.-26G=
ENST00000534397.5:c.-51+2433G=	ENSP00000432866.1:n.-51+2433G=
NM_003357.4:c.-26G=	NP_003348.1:n.-26G=
XR_950170.1:n.378-2220C=
XR_950171.1:n.234-2220C=
XR_950172.1:n.234-2220C=
XR_950173.1:n.234-2220C=
XR_950174.1:n.234-2220C=
XR_001748247.1:n.348-2220C=
XR_001748248.1:n.453-2220C=
XR_001748249.1:n.459-2220C=
XR_001748250.1:n.455-2220C=
XR_001748252.1:n.460-2220C=
XR_001748253.1:n.180-2220C=
XR_001748254.1:n.461-2220C=
XR_002957250.1:n.451-2220C=
NM_003357.5:c.-26G= MANE Select	NP_003348.1:n.-26G=