Canonical Allele Identifier: CA712945148

Gene: CDAN1

Linked Data

• dbSNP Id: rs1432388703
• MyVariant Identifiers: chr15:g.43021166A>G (hg19) ; chr15:g.42728968A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42728968A>G , CM000677.2:g.42728968A>G	GRCh38
NC_000015.9:g.43021166A>G , CM000677.1:g.43021166A>G	GRCh37
NC_000015.8:g.40808458A>G	NCBI36
NG_012491.1:g.13252T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.2645+55T>C MANE Select	ENSP00000348564.3:n.2645+55T>C
ENST00000643434.1:c.*1823+55T>C	ENSP00000494699.1:n.*1823+55T>C
ENST00000356231.3:c.2645+55T>C	ENSP00000348564.3:n.2645+55T>C
ENST00000562465.5:c.638+55T>C	ENSP00000454246.1:n.638+55T>C
NM_138477.2:c.2645+55T>C	NP_612486.2:n.2645+55T>C
XM_005254176.3:c.2648+55T>C	XP_005254233.1:n.2648+55T>C
XM_011521270.1:c.2672+55T>C	XP_011519572.1:n.2672+55T>C
XM_011521271.1:c.2669+55T>C	XP_011519573.1:n.2669+55T>C
XM_011521272.1:c.2672+55T>C	XP_011519574.1:n.2672+55T>C
XM_011521273.1:c.2672+55T>C	XP_011519575.1:n.2672+55T>C
XM_011521274.1:c.1637+55T>C	XP_011519576.1:n.1637+55T>C
XM_011521275.1:c.1889+55T>C	XP_011519577.1:n.1889+55T>C
NM_138477.4:c.2645+55T>C MANE Select	NP_612486.2:n.2645+55T>C
XM_005254176.5:c.2648+55T>C	XP_005254233.1:n.2648+55T>C
XM_011521270.2:c.2672+55T>C	XP_011519572.1:n.2672+55T>C
XM_011521271.2:c.2669+55T>C	XP_011519573.1:n.2669+55T>C
XM_011521274.2:c.1637+55T>C	XP_011519576.1:n.1637+55T>C
XR_001751104.1:n.2702+55T>C
XR_001751105.1:n.2702+55T>C