Canonical Allele Identifier: CA1272753151

Gene: CNNM4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96761491G= , CM000664.2:g.96761491G=	GRCh38
NC_000002.11:g.97427228G= , CM000664.1:g.97427228G=	GRCh37
NC_000002.10:g.96790955G=	NCBI36
NG_016608.1:g.5590G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377075.3:c.492G= MANE Select	ENSP00000366275.2:p.Thr164=
ENST00000377075.2:c.492G=	ENSP00000366275.2:p.Thr164=
NM_020184.3:c.492G=	NP_064569.3:p.Thr164=
XM_005263914.2:c.492G=	XP_005263971.1:p.Thr164=
XM_005263915.2:c.492G=	XP_005263972.1:p.Thr164=
XM_011510955.1:c.492G=	XP_011509257.1:p.Thr164=
XM_011510956.1:c.492G=	XP_011509258.1:p.Thr164=
XM_005263914.4:c.492G=	XP_005263971.1:p.Thr164=
XM_005263915.4:c.492G=	XP_005263972.1:p.Thr164=
XM_011510955.3:c.492G=	XP_011509257.1:p.Thr164=
XM_011510956.3:c.492G=	XP_011509258.1:p.Thr164=
NM_020184.4:c.492G= MANE Select	NP_064569.3:p.Thr164=