Canonical Allele Identifier: CA7515929

Gene: CDAN1

Linked Data

• dbSNP Id: rs759000974
• ExAC: 15:43023475 G / GATCTTCA
• gnomAD v2: 15-43023475-G-GATCTTCA
• gnomAD v3: 15-42731277-G-GATCTTCA
• gnomAD v4: 15-42731277-G-GATCTTCA
• MyVariant Identifiers: chr15:g.43023475_43023476insATCTTCA (hg19) ; chr15:g.42731277_42731278insATCTTCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731278_42731279insTCTTCAA , CM000677.2:g.42731278_42731279insTCTTCAA	GRCh38
NC_000015.9:g.43023476_43023477insTCTTCAA , CM000677.1:g.43023476_43023477insTCTTCAA	GRCh37
NC_000015.8:g.40810768_40810769insTCTTCAA	NCBI36
NG_012491.1:g.10942_10943insTGAAGAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.1793_1794insTGAAGAT MANE Select	ENSP00000348564.3:p.Asn599GlufsTer11
ENST00000643434.1:c.*971_*972insTGAAGAT	ENSP00000494699.1:n.*971_*972insTGAAGAT
ENST00000356231.3:c.1793_1794insTGAAGAT	ENSP00000348564.3:p.Asn599GlufsTer11
NM_138477.2:c.1793_1794insTGAAGAT	NP_612486.2:p.Asn599GlufsTer11
XM_005254176.3:c.1796_1797insTGAAGAT	XP_005254233.1:p.Asn600GlufsTer11
XM_011521270.1:c.1820_1821insTGAAGAT	XP_011519572.1:p.Asn608GlufsTer11
XM_011521271.1:c.1817_1818insTGAAGAT	XP_011519573.1:p.Asn607GlufsTer11
XM_011521272.1:c.1820_1821insTGAAGAT	XP_011519574.1:p.Asn608GlufsTer11
XM_011521273.1:c.1820_1821insTGAAGAT	XP_011519575.1:p.Asn608GlufsTer11
XM_011521274.1:c.785_786insTGAAGAT	XP_011519576.1:p.Asn263GlufsTer11
XM_011521275.1:c.1037_1038insTGAAGAT	XP_011519577.1:p.Asn347GlufsTer11
XR_931757.1:n.1831_1832insTGAAGAT
NM_138477.4:c.1793_1794insTGAAGAT MANE Select	NP_612486.2:p.Asn599GlufsTer11
XM_005254176.5:c.1796_1797insTGAAGAT	XP_005254233.1:p.Asn600GlufsTer11
XM_011521270.2:c.1820_1821insTGAAGAT	XP_011519572.1:p.Asn608GlufsTer11
XM_011521271.2:c.1817_1818insTGAAGAT	XP_011519573.1:p.Asn607GlufsTer11
XM_011521274.2:c.785_786insTGAAGAT	XP_011519576.1:p.Asn263GlufsTer11
XR_001751104.1:n.1850_1851insTGAAGAT
XR_001751105.1:n.1850_1851insTGAAGAT
XR_931757.2:n.1851_1852insTGAAGAT