Canonical Allele Identifier: CA208262341

Gene: CCAR1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68758322T>C , CM000672.2:g.68758322T>C	GRCh38
NC_000010.10:g.70518079T>C , CM000672.1:g.70518079T>C	GRCh37
NC_000010.9:g.70188085T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018237.4:c.1920+945T>C MANE Select	NP_060707.2:n.1920+945T>C
ENST00000265872.11:c.1920+945T>C MANE Select	ENSP00000265872.6:n.1920+945T>C
NM_001282959.1:c.1875+945T>C	NP_001269888.1:n.1875+945T>C
NM_001282959.2:c.1875+945T>C	NP_001269888.1:n.1875+945T>C
NM_001282960.1:c.1875+945T>C	NP_001269889.1:n.1875+945T>C
NM_001282960.2:c.1875+945T>C	NP_001269889.1:n.1875+945T>C
NM_018237.3:c.1920+945T>C	NP_060707.2:n.1920+945T>C
NR_104262.1:n.1904+945T>C
NR_104262.2:n.1809+945T>C
ENST00000265872.10:c.1920+945T>C	ENSP00000265872.6:n.1920+945T>C
ENST00000479143.2:c.252+945T>C
ENST00000536012.5:c.1335+945T>C	ENSP00000439642.1:n.1335+945T>C
ENST00000539539.5:c.1875+945T>C	ENSP00000439252.1:n.1875+945T>C
ENST00000540210.5:c.*2+945T>C	ENSP00000437760.1:n.*2+945T>C
ENST00000541012.5:c.*2+945T>C	ENSP00000439153.1:n.*2+945T>C
ENST00000543225.5:c.1842+945T>C	ENSP00000438610.1:n.1842+945T>C
ENST00000543229.5:c.*1535+945T>C	ENSP00000439571.1:n.*1535+945T>C
ENST00000543706.1:c.28+945T>C
ENST00000543719.5:c.1875+945T>C	ENSP00000445254.1:n.1875+945T>C
ENST00000630771.2:c.*2+945T>C	ENSP00000486408.1:n.*2+945T>C