Canonical Allele Identifier: CA2632683657
Gene: CORO1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30186504_30186515dup , CM000678.2:g.30186504_30186515dup GRCh38
NC_000016.9:g.30197825_30197836dup , CM000678.1:g.30197825_30197836dup GRCh37
NC_000016.8:g.30105326_30105337dup NCBI36
NG_023415.1:g.7900_7911dup , LRG_195:g.7900_7911dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696217.1:n.91_102dup
ENST00000219150.10:c.199-94_199-83dup MANE Select ENSP00000219150.6:n.199-94_199-83dup
ENST00000219150.9:c.199-94_199-83dup ENSP00000219150.5:n.199-94_199-83dup
ENST00000561815.5:c.307-94_307-83dup ENSP00000456756.1:n.307-94_307-83dup
ENST00000563778.5:c.199-94_199-83dup ENSP00000456266.1:n.199-94_199-83dup
ENST00000565497.5:c.199-94_199-83dup ENSP00000456457.1:n.199-94_199-83dup
ENST00000567034.5:n.573_584dup
ENST00000568763.1:n.1417_1428dup
ENST00000568982.5:n.317-94_317-83dup
ENST00000569203.5:c.199-94_199-83dup ENSP00000454752.1:n.199-94_199-83dup
ENST00000569469.1:n.309-94_309-83dup
ENST00000569970.1:c.199-94_199-83dup ENSP00000457509.1:n.199-94_199-83dup
ENST00000570045.5:c.199-94_199-83dup ENSP00000455552.1:n.199-94_199-83dup
ENST00000570244.5:c.199-312_199-301dup ENSP00000457332.1:n.199-312_199-301dup
NM_001193333.2:c.199-94_199-83dup NP_001180262.1:n.199-94_199-83dup
NM_007074.3:c.199-94_199-83dup NP_009005.1:n.199-94_199-83dup
XM_011545714.1:c.199-94_199-83dup XP_011544016.1:n.199-94_199-83dup
XM_011545714.2:c.199-94_199-83dup XP_011544016.1:n.199-94_199-83dup
XM_017022885.2:c.199-94_199-83dup XP_016878374.1:n.199-94_199-83dup
XM_017022886.1:c.199-94_199-83dup XP_016878375.1:n.199-94_199-83dup
NM_007074.4:c.199-94_199-83dup MANE Select NP_009005.1:n.199-94_199-83dup
NM_001193333.3:c.199-94_199-83dup NP_001180262.1:n.199-94_199-83dup