Canonical Allele Identifier: CA2628073964

Gene: CDAN1

Linked Data

• gnomAD v4: 15-42731450-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731450A>G , CM000677.2:g.42731450A>G	GRCh38
NC_000015.9:g.43023648A>G , CM000677.1:g.43023648A>G	GRCh37
NC_000015.8:g.40810940A>G	NCBI36
NG_012491.1:g.10770T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1740-119T>C MANE Select	ENSP00000348564.3:n.1740-119T>C
ENST00000643434.1:c.*918-119T>C	ENSP00000494699.1:n.*918-119T>C
ENST00000356231.3:c.1740-119T>C	ENSP00000348564.3:n.1740-119T>C
NM_138477.2:c.1740-119T>C	NP_612486.2:n.1740-119T>C
XM_005254176.3:c.1743-119T>C	XP_005254233.1:n.1743-119T>C
XM_011521270.1:c.1767-119T>C	XP_011519572.1:n.1767-119T>C
XM_011521271.1:c.1764-119T>C	XP_011519573.1:n.1764-119T>C
XM_011521272.1:c.1767-119T>C	XP_011519574.1:n.1767-119T>C
XM_011521273.1:c.1767-119T>C	XP_011519575.1:n.1767-119T>C
XM_011521274.1:c.732-119T>C	XP_011519576.1:n.732-119T>C
XM_011521275.1:c.984-119T>C	XP_011519577.1:n.984-119T>C
XR_931757.1:n.1778-119T>C
NM_138477.4:c.1740-119T>C MANE Select	NP_612486.2:n.1740-119T>C
XM_005254176.5:c.1743-119T>C	XP_005254233.1:n.1743-119T>C
XM_011521270.2:c.1767-119T>C	XP_011519572.1:n.1767-119T>C
XM_011521271.2:c.1764-119T>C	XP_011519573.1:n.1764-119T>C
XM_011521274.2:c.732-119T>C	XP_011519576.1:n.732-119T>C
XR_001751104.1:n.1797-119T>C
XR_001751105.1:n.1797-119T>C
XR_931757.2:n.1798-119T>C