Canonical Allele Identifier: CA392044918

Gene: CDAN1

Linked Data

• MyVariant Identifiers: chr15:g.43023477G>T (hg19) ; chr15:g.42731279G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731279G>T , CM000677.2:g.42731279G>T	GRCh38
NC_000015.9:g.43023477G>T , CM000677.1:g.43023477G>T	GRCh37
NC_000015.8:g.40810769G>T	NCBI36
NG_012491.1:g.10941C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1792C>A MANE Select	ENSP00000348564.3:p.Leu598Ile
ENST00000643434.1:c.*970C>A	ENSP00000494699.1:n.*970C>A
ENST00000356231.3:c.1792C>A	ENSP00000348564.3:p.Leu598Ile
NM_138477.2:c.1792C>A	NP_612486.2:p.Leu598Ile
XM_005254176.3:c.1795C>A	XP_005254233.1:p.Leu599Ile
XM_011521270.1:c.1819C>A	XP_011519572.1:p.Leu607Ile
XM_011521271.1:c.1816C>A	XP_011519573.1:p.Leu606Ile
XM_011521272.1:c.1819C>A	XP_011519574.1:p.Leu607Ile
XM_011521273.1:c.1819C>A	XP_011519575.1:p.Leu607Ile
XM_011521274.1:c.784C>A	XP_011519576.1:p.Leu262Ile
XM_011521275.1:c.1036C>A	XP_011519577.1:p.Leu346Ile
XR_931757.1:n.1830C>A
NM_138477.4:c.1792C>A MANE Select	NP_612486.2:p.Leu598Ile
XM_005254176.5:c.1795C>A	XP_005254233.1:p.Leu599Ile
XM_011521270.2:c.1819C>A	XP_011519572.1:p.Leu607Ile
XM_011521271.2:c.1816C>A	XP_011519573.1:p.Leu606Ile
XM_011521274.2:c.784C>A	XP_011519576.1:p.Leu262Ile
XR_001751104.1:n.1849C>A
XR_001751105.1:n.1849C>A
XR_931757.2:n.1850C>A