Canonical Allele Identifier: CA269905898

Gene: CDAN1

Linked Data

• dbSNP Id: rs113785811
• gnomAD v2: 15-43023670-C-T
• gnomAD v3: 15-42731472-C-T
• gnomAD v4: 15-42731472-C-T
• MyVariant Identifiers: chr15:g.43023670C>T (hg19) ; chr15:g.42731472C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731472C>T , CM000677.2:g.42731472C>T	GRCh38
NC_000015.9:g.43023670C>T , CM000677.1:g.43023670C>T	GRCh37
NC_000015.8:g.40810962C>T	NCBI36
NG_012491.1:g.10748G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1740-141G>A MANE Select	ENSP00000348564.3:n.1740-141G>A
ENST00000643434.1:c.*918-141G>A	ENSP00000494699.1:n.*918-141G>A
ENST00000356231.3:c.1740-141G>A	ENSP00000348564.3:n.1740-141G>A
NM_138477.2:c.1740-141G>A	NP_612486.2:n.1740-141G>A
XM_005254176.3:c.1743-141G>A	XP_005254233.1:n.1743-141G>A
XM_011521270.1:c.1767-141G>A	XP_011519572.1:n.1767-141G>A
XM_011521271.1:c.1764-141G>A	XP_011519573.1:n.1764-141G>A
XM_011521272.1:c.1767-141G>A	XP_011519574.1:n.1767-141G>A
XM_011521273.1:c.1767-141G>A	XP_011519575.1:n.1767-141G>A
XM_011521274.1:c.732-141G>A	XP_011519576.1:n.732-141G>A
XM_011521275.1:c.984-141G>A	XP_011519577.1:n.984-141G>A
XR_931757.1:n.1778-141G>A
NM_138477.4:c.1740-141G>A MANE Select	NP_612486.2:n.1740-141G>A
XM_005254176.5:c.1743-141G>A	XP_005254233.1:n.1743-141G>A
XM_011521270.2:c.1767-141G>A	XP_011519572.1:n.1767-141G>A
XM_011521271.2:c.1764-141G>A	XP_011519573.1:n.1764-141G>A
XM_011521274.2:c.732-141G>A	XP_011519576.1:n.732-141G>A
XR_001751104.1:n.1797-141G>A
XR_001751105.1:n.1797-141G>A
XR_931757.2:n.1798-141G>A