Canonical Allele Identifier: CA2620676728

Gene: CRY1

Linked Data

• gnomAD v4: 12-107001354-CAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.107001355_107001356del , CM000674.2:g.107001355_107001356del	GRCh38
NC_000012.11:g.107395133_107395134del , CM000674.1:g.107395133_107395134del	GRCh37
NC_000012.10:g.105919263_105919264del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000008527.10:c.608_609del MANE Select	ENSP00000008527.5:p.Asp203GlyfsTer13
ENST00000008527.9:c.608_609del	ENSP00000008527.5:p.Asp203GlyfsTer13
ENST00000546722.1:n.101_102del
ENST00000552790.5:n.1167_1168del
NM_004075.4:c.608_609del	NP_004066.1:p.Asp203GlyfsTer13
XM_011537939.1:c.524_525del	XP_011536241.1:p.Asp175GlyfsTer13
XM_017018832.2:c.524_525del	XP_016874321.1:p.Asp175GlyfsTer13
XM_024448844.1:c.608_609del	XP_024304612.1:p.Asp203GlyfsTer13
XM_024448845.1:c.524_525del	XP_024304613.1:p.Asp175GlyfsTer13
NM_004075.5:c.608_609del MANE Select	NP_004066.1:p.Asp203GlyfsTer13