Canonical Allele Identifier: CA2216454750

Gene: CORO1A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30186762_30186767delinsAGGATG , CM000678.2:g.30186762_30186767delinsAGGATG	GRCh38
NC_000016.9:g.30198083_30198088delinsAGGATG , CM000678.1:g.30198083_30198088delinsAGGATG	GRCh37
NC_000016.8:g.30105584_30105589delinsAGGATG	NCBI36
NG_023415.1:g.8158_8163delinsAGGATG , LRG_195:g.8158_8163delinsAGGATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696217.1:n.349_354delinsAGGATG
ENST00000219150.10:c.321+42_321+47delinsAGGATG MANE Select	ENSP00000219150.6:n.321+42_321+47delinsAGGATG
ENST00000219150.9:c.321+42_321+47delinsAGGATG	ENSP00000219150.5:n.321+42_321+47delinsAGGATG
ENST00000561815.5:c.429+42_429+47delinsAGGATG	ENSP00000456756.1:n.429+42_429+47delinsAGGATG
ENST00000563778.5:c.321+42_321+47delinsAGGATG	ENSP00000456266.1:n.321+42_321+47delinsAGGATG
ENST00000564768.1:n.81_86delinsAGGATG
ENST00000565497.5:c.321+42_321+47delinsAGGATG	ENSP00000456457.1:n.321+42_321+47delinsAGGATG
ENST00000567034.5:n.789+42_789+47delinsAGGATG
ENST00000568763.1:n.1633+42_1633+47delinsAGGATG
ENST00000568982.5:n.439+42_439+47delinsAGGATG
ENST00000569203.5:c.321+42_321+47delinsAGGATG	ENSP00000454752.1:n.321+42_321+47delinsAGGATG
ENST00000569469.1:n.431+42_431+47delinsAGGATG
ENST00000569970.1:c.321+42_321+47delinsAGGATG	ENSP00000457509.1:n.321+42_321+47delinsAGGATG
ENST00000570045.5:c.321+42_321+47delinsAGGATG	ENSP00000455552.1:n.321+42_321+47delinsAGGATG
ENST00000570244.5:c.199-54_199-49delinsAGGATG	ENSP00000457332.1:n.199-54_199-49delinsAGGATG
NM_001193333.2:c.321+42_321+47delinsAGGATG	NP_001180262.1:n.321+42_321+47delinsAGGATG
NM_007074.3:c.321+42_321+47delinsAGGATG	NP_009005.1:n.321+42_321+47delinsAGGATG
XM_011545714.1:c.321+42_321+47delinsAGGATG	XP_011544016.1:n.321+42_321+47delinsAGGATG
XM_011545714.2:c.321+42_321+47delinsAGGATG	XP_011544016.1:n.321+42_321+47delinsAGGATG
XM_017022885.2:c.321+42_321+47delinsAGGATG	XP_016878374.1:n.321+42_321+47delinsAGGATG
XM_017022886.1:c.321+42_321+47delinsAGGATG	XP_016878375.1:n.321+42_321+47delinsAGGATG
NM_007074.4:c.321+42_321+47delinsAGGATG MANE Select	NP_009005.1:n.321+42_321+47delinsAGGATG
NM_001193333.3:c.321+42_321+47delinsAGGATG	NP_001180262.1:n.321+42_321+47delinsAGGATG