Canonical Allele Identifier: CA621826684

Gene: CORO1A

Linked Data

• dbSNP Id: rs1319177821
• gnomAD v2: 16-30198045-AGTG-A
• MyVariant Identifiers: chr16:g.30198046_30198048del (hg19) ; chr16:g.30186725_30186727del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186732_30186734del , CM000678.2:g.30186732_30186734del	GRCh38
NC_000016.9:g.30198053_30198055del , CM000678.1:g.30198053_30198055del	GRCh37
NC_000016.8:g.30105554_30105556del	NCBI36
NG_023415.1:g.8128_8130del , LRG_195:g.8128_8130del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.319_321del
ENST00000219150.10:c.321+12_321+14del MANE Select	ENSP00000219150.6:n.321+12_321+14del
ENST00000219150.9:c.321+12_321+14del	ENSP00000219150.5:n.321+12_321+14del
ENST00000561815.5:c.429+12_429+14del	ENSP00000456756.1:n.429+12_429+14del
ENST00000563778.5:c.321+12_321+14del	ENSP00000456266.1:n.321+12_321+14del
ENST00000564768.1:n.51_53del
ENST00000565497.5:c.321+12_321+14del	ENSP00000456457.1:n.321+12_321+14del
ENST00000567034.5:n.789+12_789+14del
ENST00000568763.1:n.1633+12_1633+14del
ENST00000568982.5:n.439+12_439+14del
ENST00000569203.5:c.321+12_321+14del	ENSP00000454752.1:n.321+12_321+14del
ENST00000569469.1:n.431+12_431+14del
ENST00000569970.1:c.321+12_321+14del	ENSP00000457509.1:n.321+12_321+14del
ENST00000570045.5:c.321+12_321+14del	ENSP00000455552.1:n.321+12_321+14del
ENST00000570244.5:c.199-84_199-82del	ENSP00000457332.1:n.199-84_199-82del
NM_001193333.2:c.321+12_321+14del	NP_001180262.1:n.321+12_321+14del
NM_007074.3:c.321+12_321+14del	NP_009005.1:n.321+12_321+14del
XM_011545714.1:c.321+12_321+14del	XP_011544016.1:n.321+12_321+14del
XM_011545714.2:c.321+12_321+14del	XP_011544016.1:n.321+12_321+14del
XM_017022885.2:c.321+12_321+14del	XP_016878374.1:n.321+12_321+14del
XM_017022886.1:c.321+12_321+14del	XP_016878375.1:n.321+12_321+14del
NM_007074.4:c.321+12_321+14del MANE Select	NP_009005.1:n.321+12_321+14del
NM_001193333.3:c.321+12_321+14del	NP_001180262.1:n.321+12_321+14del