Canonical Allele Identifier: CA2632683673
Gene: CORO1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30186518_30186527dup , CM000678.2:g.30186518_30186527dup GRCh38
NC_000016.9:g.30197839_30197848dup , CM000678.1:g.30197839_30197848dup GRCh37
NC_000016.8:g.30105340_30105349dup NCBI36
NG_023415.1:g.7914_7923dup , LRG_195:g.7914_7923dup

Transcript Alleles

HGVS Amino-acid change
ENST00000696217.1:n.105_114dup
ENST00000219150.10:c.199-80_199-71dup MANE Select ENSP00000219150.6:n.199-80_199-71dup
ENST00000219150.9:c.199-80_199-71dup ENSP00000219150.5:n.199-80_199-71dup
ENST00000561815.5:c.307-80_307-71dup ENSP00000456756.1:n.307-80_307-71dup
ENST00000563778.5:c.199-80_199-71dup ENSP00000456266.1:n.199-80_199-71dup
ENST00000565497.5:c.199-80_199-71dup ENSP00000456457.1:n.199-80_199-71dup
ENST00000567034.5:n.587_596dup
ENST00000568763.1:n.1431_1440dup
ENST00000568982.5:n.317-80_317-71dup
ENST00000569203.5:c.199-80_199-71dup ENSP00000454752.1:n.199-80_199-71dup
ENST00000569469.1:n.309-80_309-71dup
ENST00000569970.1:c.199-80_199-71dup ENSP00000457509.1:n.199-80_199-71dup
ENST00000570045.5:c.199-80_199-71dup ENSP00000455552.1:n.199-80_199-71dup
ENST00000570244.5:c.199-298_199-289dup ENSP00000457332.1:n.199-298_199-289dup
NM_001193333.2:c.199-80_199-71dup NP_001180262.1:n.199-80_199-71dup
NM_007074.3:c.199-80_199-71dup NP_009005.1:n.199-80_199-71dup
XM_011545714.1:c.199-80_199-71dup XP_011544016.1:n.199-80_199-71dup
XM_011545714.2:c.199-80_199-71dup XP_011544016.1:n.199-80_199-71dup
XM_017022885.2:c.199-80_199-71dup XP_016878374.1:n.199-80_199-71dup
XM_017022886.1:c.199-80_199-71dup XP_016878375.1:n.199-80_199-71dup
NM_007074.4:c.199-80_199-71dup MANE Select NP_009005.1:n.199-80_199-71dup
NM_001193333.3:c.199-80_199-71dup NP_001180262.1:n.199-80_199-71dup