Canonical Allele Identifier: CA269905949

Gene: CDAN1

Linked Data

• dbSNP Id: rs1056000177
• gnomAD v2: 15-43023716-C-A
• gnomAD v3: 15-42731518-C-A
• gnomAD v4: 15-42731518-C-A
• MyVariant Identifiers: chr15:g.43023716C>A (hg19) ; chr15:g.42731518C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731518C>A , CM000677.2:g.42731518C>A	GRCh38
NC_000015.9:g.43023716C>A , CM000677.1:g.43023716C>A	GRCh37
NC_000015.8:g.40811008C>A	NCBI36
NG_012491.1:g.10702G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1739+102G>T MANE Select	ENSP00000348564.3:n.1739+102G>T
ENST00000643434.1:c.*917+102G>T	ENSP00000494699.1:n.*917+102G>T
ENST00000356231.3:c.1739+102G>T	ENSP00000348564.3:n.1739+102G>T
NM_138477.2:c.1739+102G>T	NP_612486.2:n.1739+102G>T
XM_005254176.3:c.1742+102G>T	XP_005254233.1:n.1742+102G>T
XM_011521270.1:c.1766+102G>T	XP_011519572.1:n.1766+102G>T
XM_011521271.1:c.1763+102G>T	XP_011519573.1:n.1763+102G>T
XM_011521272.1:c.1766+102G>T	XP_011519574.1:n.1766+102G>T
XM_011521273.1:c.1766+102G>T	XP_011519575.1:n.1766+102G>T
XM_011521274.1:c.731+102G>T	XP_011519576.1:n.731+102G>T
XM_011521275.1:c.983+102G>T	XP_011519577.1:n.983+102G>T
XR_931757.1:n.1777+102G>T
NM_138477.4:c.1739+102G>T MANE Select	NP_612486.2:n.1739+102G>T
XM_005254176.5:c.1742+102G>T	XP_005254233.1:n.1742+102G>T
XM_011521270.2:c.1766+102G>T	XP_011519572.1:n.1766+102G>T
XM_011521271.2:c.1763+102G>T	XP_011519573.1:n.1763+102G>T
XM_011521274.2:c.731+102G>T	XP_011519576.1:n.731+102G>T
XR_001751104.1:n.1796+102G>T
XR_001751105.1:n.1796+102G>T
XR_931757.2:n.1797+102G>T