Canonical Allele Identifier: CA715938

Gene: AHDC1

Linked Data

• ClinVar Variation Id: 381724
• ClinVar RCV Id: RCV000433811
• dbSNP Id: rs367582615
• ExAC: 1:27877168 G / A
• gnomAD v2: 1-27877168-G-A
• gnomAD v4: 1-27550657-G-A
• COSMIC: COSM907899
• MyVariant Identifiers: chr1:g.27877168G>A (hg19) ; chr1:g.27877168_27877169delinsAC (hg19) ; chr1:g.27550657G>A (hg38) ; chr1:g.27550657_27550658delinsAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.27550657G>A , CM000663.2:g.27550657G>A	GRCh38
NC_000001.10:g.27877168G>A , CM000663.1:g.27877168G>A	GRCh37
NC_000001.9:g.27749755G>A	NCBI36
NG_034158.1:g.57838C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247087.10:c.1459C>T	ENSP00000247087.4:p.Arg487Trp
ENST00000642245.1:c.1459C>T	ENSP00000495072.1:p.Arg487Trp
ENST00000642416.1:c.1459C>T	ENSP00000494394.1:p.Arg487Trp
ENST00000644989.1:c.1459C>T	ENSP00000495665.1:p.Arg487Trp
ENST00000673934.1:c.1459C>T MANE Select	ENSP00000501218.1:p.Arg487Trp
ENST00000247087.9:c.1459C>T	ENSP00000247087.4:p.Arg487Trp
ENST00000374011.6:c.1459C>T	ENSP00000363123.2:p.Arg487Trp
NM_001029882.3:c.1459C>T	NP_001025053.1:p.Arg487Trp
XM_005245848.2:c.1459C>T	XP_005245905.1:p.Arg487Trp
XM_005245849.2:c.1459C>T	XP_005245906.1:p.Arg487Trp
XM_005245850.2:c.1459C>T	XP_005245907.1:p.Arg487Trp
XM_005245851.2:c.1459C>T	XP_005245908.1:p.Arg487Trp
XM_005245852.2:c.1459C>T	XP_005245909.1:p.Arg487Trp
XM_011541255.1:c.1459C>T	XP_011539557.1:p.Arg487Trp
XM_011541256.1:c.1459C>T	XP_011539558.1:p.Arg487Trp
XM_011541257.1:c.1459C>T	XP_011539559.1:p.Arg487Trp
XR_946609.1:n.2416C>T
XM_005245848.3:c.1459C>T	XP_005245905.1:p.Arg487Trp
XM_005245849.3:c.1459C>T	XP_005245906.1:p.Arg487Trp
XM_005245850.3:c.1459C>T	XP_005245907.1:p.Arg487Trp
XM_005245851.3:c.1459C>T	XP_005245908.1:p.Arg487Trp
XM_005245852.3:c.1459C>T	XP_005245909.1:p.Arg487Trp
XM_011541256.2:c.1459C>T	XP_011539558.1:p.Arg487Trp
XM_011541257.2:c.1459C>T	XP_011539559.1:p.Arg487Trp
XM_024446461.1:c.1459C>T	XP_024302229.1:p.Arg487Trp
XR_946609.2:n.2526C>T
NM_001371928.1:c.1459C>T MANE Select	NP_001358857.1:p.Arg487Trp