Canonical Allele Identifier: CA2632684518
Gene: CORO1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30186934_30186938dup , CM000678.2:g.30186934_30186938dup GRCh38
NC_000016.9:g.30198255_30198259dup , CM000678.1:g.30198255_30198259dup GRCh37
NC_000016.8:g.30105756_30105760dup NCBI36
NG_023415.1:g.8330_8334dup , LRG_195:g.8330_8334dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696217.1:n.521_525dup
ENST00000219150.10:c.440_444dup MANE Select ENSP00000219150.6:p.Ser149CysfsTer9
ENST00000219150.9:c.440_444dup ENSP00000219150.5:p.Ser149CysfsTer9
ENST00000561815.5:c.548_552dup ENSP00000456756.1:p.Ser185CysfsTer9
ENST00000563778.5:c.440_444dup ENSP00000456266.1:p.Ser149CysfsTer9
ENST00000564768.1:n.253_257dup
ENST00000565497.5:c.440_444dup ENSP00000456457.1:p.Ser149CysfsTer9
ENST00000567034.5:n.908_912dup
ENST00000568763.1:n.1752_1756dup
ENST00000568982.5:n.558_562dup
ENST00000569469.1:n.432-105_432-101dup
ENST00000569970.1:c.440_444dup ENSP00000457509.1:p.Ser149CysfsTer9
ENST00000570045.5:c.440_444dup ENSP00000455552.1:p.Ser149CysfsTer9
ENST00000570244.5:c.317_321dup ENSP00000457332.1:p.Ser108CysfsTer9
NM_001193333.2:c.440_444dup NP_001180262.1:p.Ser149CysfsTer9
NM_007074.3:c.440_444dup NP_009005.1:p.Ser149CysfsTer9
XM_011545714.1:c.440_444dup XP_011544016.1:p.Ser149CysfsTer9
XM_011545714.2:c.440_444dup XP_011544016.1:p.Ser149CysfsTer9
XM_017022885.2:c.440_444dup XP_016878374.1:p.Ser149CysfsTer9
XM_017022886.1:c.440_444dup XP_016878375.1:p.Ser149CysfsTer9
NM_007074.4:c.440_444dup MANE Select NP_009005.1:p.Ser149CysfsTer9
NM_001193333.3:c.440_444dup NP_001180262.1:p.Ser149CysfsTer9