Canonical Allele Identifier: CA2660221303

Gene: CNNM4

Linked Data

• gnomAD v4: 2-96761462-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96761463dup , CM000664.2:g.96761463dup	GRCh38
NC_000002.11:g.97427200dup , CM000664.1:g.97427200dup	GRCh37
NC_000002.10:g.96790927dup	NCBI36
NG_016608.1:g.5562dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377075.3:c.464dup MANE Select	ENSP00000366275.2:p.Pro156AlafsTer?
ENST00000377075.2:c.464dup	ENSP00000366275.2:p.Pro156AlafsTer?
NM_020184.3:c.464dup	NP_064569.3:p.Pro156AlafsTer?
XM_005263914.2:c.464dup	XP_005263971.1:p.Pro156AlafsTer?
XM_005263915.2:c.464dup	XP_005263972.1:p.Pro156AlafsTer?
XM_011510955.1:c.464dup	XP_011509257.1:p.Pro156AlafsTer?
XM_011510956.1:c.464dup	XP_011509258.1:p.Pro156AlafsTer?
XM_005263914.4:c.464dup	XP_005263971.1:p.Pro156AlafsTer?
XM_005263915.4:c.464dup	XP_005263972.1:p.Pro156AlafsTer?
XM_011510955.3:c.464dup	XP_011509257.1:p.Pro156AlafsTer?
XM_011510956.3:c.464dup	XP_011509258.1:p.Pro156AlafsTer?
NM_020184.4:c.464dup MANE Select	NP_064569.3:p.Pro156AlafsTer?