Canonical Allele Identifier: CA715772

Gene: AHDC1

Linked Data

• ClinVar Variation Id: 1694502
• ClinVar RCV Id: RCV002262222
• dbSNP Id: rs746453956
• ExAC: 1:27876232 G / T
• gnomAD v2: 1-27876232-G-T
• gnomAD v3: 1-27549721-G-T
• gnomAD v4: 1-27549721-G-T
• COSMIC: COSM3487708
• MyVariant Identifiers: chr1:g.27876232G>T (hg19) ; chr1:g.27549721G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.27549721G>T , CM000663.2:g.27549721G>T	GRCh38
NC_000001.10:g.27876232G>T , CM000663.1:g.27876232G>T	GRCh37
NC_000001.9:g.27748819G>T	NCBI36
NG_034158.1:g.58774C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247087.10:c.2395C>A	ENSP00000247087.4:p.Arg799=
ENST00000642245.1:c.2395C>A	ENSP00000495072.1:p.Arg799=
ENST00000642416.1:c.2395C>A	ENSP00000494394.1:p.Arg799=
ENST00000644989.1:c.2395C>A	ENSP00000495665.1:p.Arg799=
ENST00000673934.1:c.2395C>A MANE Select	ENSP00000501218.1:p.Arg799=
ENST00000247087.9:c.2395C>A	ENSP00000247087.4:p.Arg799=
ENST00000374011.6:c.2395C>A	ENSP00000363123.2:p.Arg799=
NM_001029882.3:c.2395C>A	NP_001025053.1:p.Arg799=
XM_005245848.2:c.2395C>A	XP_005245905.1:p.Arg799=
XM_005245849.2:c.2395C>A	XP_005245906.1:p.Arg799=
XM_005245850.2:c.2395C>A	XP_005245907.1:p.Arg799=
XM_005245851.2:c.2395C>A	XP_005245908.1:p.Arg799=
XM_005245852.2:c.2395C>A	XP_005245909.1:p.Arg799=
XM_011541255.1:c.2395C>A	XP_011539557.1:p.Arg799=
XM_011541256.1:c.2395C>A	XP_011539558.1:p.Arg799=
XM_011541257.1:c.2395C>A	XP_011539559.1:p.Arg799=
XR_946609.1:n.3352C>A
XM_005245848.3:c.2395C>A	XP_005245905.1:p.Arg799=
XM_005245849.3:c.2395C>A	XP_005245906.1:p.Arg799=
XM_005245850.3:c.2395C>A	XP_005245907.1:p.Arg799=
XM_005245851.3:c.2395C>A	XP_005245908.1:p.Arg799=
XM_005245852.3:c.2395C>A	XP_005245909.1:p.Arg799=
XM_011541256.2:c.2395C>A	XP_011539558.1:p.Arg799=
XM_011541257.2:c.2395C>A	XP_011539559.1:p.Arg799=
XM_024446461.1:c.2395C>A	XP_024302229.1:p.Arg799=
XR_946609.2:n.3462C>A
NM_001371928.1:c.2395C>A MANE Select	NP_001358857.1:p.Arg799=