Canonical Allele Identifier: CA1272770214

Gene: CNNM4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96799065C= , CM000664.2:g.96799065C=	GRCh38
NC_000002.11:g.97464802C= , CM000664.1:g.97464802C=	GRCh37
NC_000002.10:g.96828529C=	NCBI36
NG_016608.1:g.43164C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377075.3:c.1690C= MANE Select	ENSP00000366275.2:p.Gln564=
ENST00000377075.2:c.1690C=	ENSP00000366275.2:p.Gln564=
ENST00000493384.1:n.470C=
ENST00000496186.5:n.364C=
NM_020184.3:c.1690C=	NP_064569.3:p.Gln564=
XM_005263914.2:c.1690C=	XP_005263971.1:p.Gln564=
XM_005263915.2:c.1690C=	XP_005263972.1:p.Gln564=
XM_011510955.1:c.1690C=	XP_011509257.1:p.Gln564=
XM_005263914.4:c.1690C=	XP_005263971.1:p.Gln564=
XM_005263915.4:c.1690C=	XP_005263972.1:p.Gln564=
XM_011510955.3:c.1690C=	XP_011509257.1:p.Gln564=
XM_017003799.1:c.151C=	XP_016859288.1:p.Gln51=
NM_020184.4:c.1690C= MANE Select	NP_064569.3:p.Gln564=