Canonical Allele Identifier: CA1783200

Gene: CNNM4

Linked Data

• ClinVar Variation Id: 1596082
• ClinVar RCV Id: RCV002117275
• dbSNP Id: rs760053491
• ExAC: 2:97427141 C / T
• gnomAD v2: 2-97427141-C-T
• gnomAD v3: 2-96761404-C-T
• gnomAD v4: 2-96761404-C-T
• MyVariant Identifiers: chr2:g.97427141C>T (hg19) ; chr2:g.96761404C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96761404C>T , CM000664.2:g.96761404C>T	GRCh38
NC_000002.11:g.97427141C>T , CM000664.1:g.97427141C>T	GRCh37
NC_000002.10:g.96790868C>T	NCBI36
NG_016608.1:g.5503C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377075.3:c.405C>T MANE Select	ENSP00000366275.2:p.Leu135=
ENST00000377075.2:c.405C>T	ENSP00000366275.2:p.Leu135=
NM_020184.3:c.405C>T	NP_064569.3:p.Leu135=
XM_005263914.2:c.405C>T	XP_005263971.1:p.Leu135=
XM_005263915.2:c.405C>T	XP_005263972.1:p.Leu135=
XM_011510955.1:c.405C>T	XP_011509257.1:p.Leu135=
XM_011510956.1:c.405C>T	XP_011509258.1:p.Leu135=
XM_005263914.4:c.405C>T	XP_005263971.1:p.Leu135=
XM_005263915.4:c.405C>T	XP_005263972.1:p.Leu135=
XM_011510955.3:c.405C>T	XP_011509257.1:p.Leu135=
XM_011510956.3:c.405C>T	XP_011509258.1:p.Leu135=
NM_020184.4:c.405C>T MANE Select	NP_064569.3:p.Leu135=