Canonical Allele Identifier: CA715829

Gene: AHDC1

Linked Data

• ClinVar Variation Id: 1896402
• ClinVar RCV Id: RCV002575178
• dbSNP Id: rs559351156
• ExAC: 1:27876491 G / A
• gnomAD v2: 1-27876491-G-A
• gnomAD v3: 1-27549980-G-A
• gnomAD v4: 1-27549980-G-A
• MyVariant Identifiers: chr1:g.27876491G>A (hg19) ; chr1:g.27549980G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.27549980G>A , CM000663.2:g.27549980G>A	GRCh38
NC_000001.10:g.27876491G>A , CM000663.1:g.27876491G>A	GRCh37
NC_000001.9:g.27749078G>A	NCBI36
NG_034158.1:g.58515C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247087.10:c.2136C>T	ENSP00000247087.4:p.Val712=
ENST00000642245.1:c.2136C>T	ENSP00000495072.1:p.Val712=
ENST00000642416.1:c.2136C>T	ENSP00000494394.1:p.Val712=
ENST00000644989.1:c.2136C>T	ENSP00000495665.1:p.Val712=
ENST00000673934.1:c.2136C>T MANE Select	ENSP00000501218.1:p.Val712=
ENST00000247087.9:c.2136C>T	ENSP00000247087.4:p.Val712=
ENST00000374011.6:c.2136C>T	ENSP00000363123.2:p.Val712=
NM_001029882.3:c.2136C>T	NP_001025053.1:p.Val712=
XM_005245848.2:c.2136C>T	XP_005245905.1:p.Val712=
XM_005245849.2:c.2136C>T	XP_005245906.1:p.Val712=
XM_005245850.2:c.2136C>T	XP_005245907.1:p.Val712=
XM_005245851.2:c.2136C>T	XP_005245908.1:p.Val712=
XM_005245852.2:c.2136C>T	XP_005245909.1:p.Val712=
XM_011541255.1:c.2136C>T	XP_011539557.1:p.Val712=
XM_011541256.1:c.2136C>T	XP_011539558.1:p.Val712=
XM_011541257.1:c.2136C>T	XP_011539559.1:p.Val712=
XR_946609.1:n.3093C>T
XM_005245848.3:c.2136C>T	XP_005245905.1:p.Val712=
XM_005245849.3:c.2136C>T	XP_005245906.1:p.Val712=
XM_005245850.3:c.2136C>T	XP_005245907.1:p.Val712=
XM_005245851.3:c.2136C>T	XP_005245908.1:p.Val712=
XM_005245852.3:c.2136C>T	XP_005245909.1:p.Val712=
XM_011541256.2:c.2136C>T	XP_011539558.1:p.Val712=
XM_011541257.2:c.2136C>T	XP_011539559.1:p.Val712=
XM_024446461.1:c.2136C>T	XP_024302229.1:p.Val712=
XR_946609.2:n.3203C>T
NM_001371928.1:c.2136C>T MANE Select	NP_001358857.1:p.Val712=