Canonical Allele Identifier: CA2620676676

Gene: CRY1

Linked Data

• gnomAD v4: 12-107001176-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001180dup , CM000674.2:g.107001180dup	GRCh38
NC_000012.11:g.107394958dup , CM000674.1:g.107394958dup	GRCh37
NC_000012.10:g.105919088dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.684+103dup MANE Select	ENSP00000008527.5:n.684+103dup
ENST00000008527.9:c.684+103dup	ENSP00000008527.5:n.684+103dup
ENST00000546722.1:n.177+103dup
ENST00000552790.5:n.1243+103dup
NM_004075.4:c.684+103dup	NP_004066.1:n.684+103dup
XM_011537939.1:c.600+103dup	XP_011536241.1:n.600+103dup
XM_017018832.2:c.600+103dup	XP_016874321.1:n.600+103dup
XM_024448844.1:c.684+103dup	XP_024304612.1:n.684+103dup
XM_024448845.1:c.600+103dup	XP_024304613.1:n.600+103dup
NM_004075.5:c.684+103dup MANE Select	NP_004066.1:n.684+103dup