Canonical Allele Identifier: CA2012806558
Gene: CRACR2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3648382T>G , CM000674.2:g.3648382T>G GRCh38
NC_000012.11:g.3757548T>G , CM000674.1:g.3757548T>G GRCh37
NC_000012.10:g.3627809T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000440314.7:c.1118+160A>C MANE Select ENSP00000409382.2:n.1118+160A>C
ENST00000252322.1:c.*90A>C ENSP00000252322.1:n.*90A>C
ENST00000333750.9:c.686A>C
ENST00000440314.6:c.1118+160A>C ENSP00000409382.2:n.1118+160A>C
ENST00000535292.1:c.84+160A>C
NM_001144958.1:c.1118+160A>C NP_001138430.1:n.1118+160A>C
NM_032680.3:c.*90A>C NP_116069.1:n.*90A>C
XM_006719021.2:c.1118+160A>C XP_006719084.1:n.1118+160A>C
XM_011521034.1:c.1118+160A>C XP_011519336.1:n.1118+160A>C
XM_011521035.1:c.1118+160A>C XP_011519337.1:n.1118+160A>C
XM_011521036.1:c.1118+160A>C XP_011519338.1:n.1118+160A>C
XM_011521037.1:c.401+160A>C XP_011519339.1:n.401+160A>C
XM_011521038.1:c.401+160A>C XP_011519340.1:n.401+160A>C
XM_006719021.3:c.1118+160A>C XP_006719084.1:n.1118+160A>C
XM_011521034.3:c.1118+160A>C XP_011519336.1:n.1118+160A>C
XM_011521036.3:c.1118+160A>C XP_011519338.1:n.1118+160A>C
XM_011521037.2:c.401+160A>C XP_011519339.1:n.401+160A>C
XM_011521038.2:c.401+160A>C XP_011519340.1:n.401+160A>C
NM_001144958.2:c.1118+160A>C MANE Select NP_001138430.1:n.1118+160A>C
NM_032680.4:c.*90A>C NP_116069.1:n.*90A>C