Canonical Allele Identifier: CA427813298

Gene: CNNM4

Linked Data

• MyVariant Identifiers: chr2:g.97427294T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96761557T>C , CM000664.2:g.96761557T>C	GRCh38
NC_000002.11:g.97427294T>C , CM000664.1:g.97427294T>C	GRCh37
NC_000002.10:g.96791021T>C	NCBI36
NG_016608.1:g.5656T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377075.3:c.558T>C MANE Select	ENSP00000366275.2:p.Ile186=
ENST00000377075.2:c.558T>C	ENSP00000366275.2:p.Ile186=
NM_020184.3:c.558T>C	NP_064569.3:p.Ile186=
XM_005263914.2:c.558T>C	XP_005263971.1:p.Ile186=
XM_005263915.2:c.558T>C	XP_005263972.1:p.Ile186=
XM_011510955.1:c.558T>C	XP_011509257.1:p.Ile186=
XM_011510956.1:c.558T>C	XP_011509258.1:p.Ile186=
XM_005263914.4:c.558T>C	XP_005263971.1:p.Ile186=
XM_005263915.4:c.558T>C	XP_005263972.1:p.Ile186=
XM_011510955.3:c.558T>C	XP_011509257.1:p.Ile186=
XM_011510956.3:c.558T>C	XP_011509258.1:p.Ile186=
NM_020184.4:c.558T>C MANE Select	NP_064569.3:p.Ile186=