Canonical Allele Identifier: CA2660221305

Gene: CNNM4

Linked Data

• gnomAD v4: 2-96761641-G-GCA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96761642_96761643insAC , CM000664.2:g.96761642_96761643insAC	GRCh38
NC_000002.11:g.97427379_97427380insAC , CM000664.1:g.97427379_97427380insAC	GRCh37
NC_000002.10:g.96791106_96791107insAC	NCBI36
NG_016608.1:g.5741_5742insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377075.3:c.643_644insAC MANE Select	ENSP00000366275.2:p.Arg215HisfsTer?
ENST00000377075.2:c.643_644insAC	ENSP00000366275.2:p.Arg215HisfsTer?
NM_020184.3:c.643_644insAC	NP_064569.3:p.Arg215HisfsTer?
XM_005263914.2:c.643_644insAC	XP_005263971.1:p.Arg215HisfsTer?
XM_005263915.2:c.643_644insAC	XP_005263972.1:p.Arg215HisfsTer?
XM_011510955.1:c.643_644insAC	XP_011509257.1:p.Arg215HisfsTer?
XM_011510956.1:c.643_644insAC	XP_011509258.1:p.Arg215HisfsTer?
XM_005263914.4:c.643_644insAC	XP_005263971.1:p.Arg215HisfsTer?
XM_005263915.4:c.643_644insAC	XP_005263972.1:p.Arg215HisfsTer?
XM_011510955.3:c.643_644insAC	XP_011509257.1:p.Arg215HisfsTer?
XM_011510956.3:c.643_644insAC	XP_011509258.1:p.Arg215HisfsTer?
NM_020184.4:c.643_644insAC MANE Select	NP_064569.3:p.Arg215HisfsTer?