Canonical Allele Identifier: CA1272753198

Gene: CNNM4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96761580T= , CM000664.2:g.96761580T=	GRCh38
NC_000002.11:g.97427317T= , CM000664.1:g.97427317T=	GRCh37
NC_000002.10:g.96791044T=	NCBI36
NG_016608.1:g.5679T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377075.3:c.581T= MANE Select	ENSP00000366275.2:p.Val194=
ENST00000377075.2:c.581T=	ENSP00000366275.2:p.Val194=
NM_020184.3:c.581T=	NP_064569.3:p.Val194=
XM_005263914.2:c.581T=	XP_005263971.1:p.Val194=
XM_005263915.2:c.581T=	XP_005263972.1:p.Val194=
XM_011510955.1:c.581T=	XP_011509257.1:p.Val194=
XM_011510956.1:c.581T=	XP_011509258.1:p.Val194=
XM_005263914.4:c.581T=	XP_005263971.1:p.Val194=
XM_005263915.4:c.581T=	XP_005263972.1:p.Val194=
XM_011510955.3:c.581T=	XP_011509257.1:p.Val194=
XM_011510956.3:c.581T=	XP_011509258.1:p.Val194=
NM_020184.4:c.581T= MANE Select	NP_064569.3:p.Val194=