Canonical Allele Identifier: CA339229995

Gene: AHDC1

Linked Data

• COSMIC: COSM4031135
• MyVariant Identifiers: chr1:g.27875931G>A (hg19) ; chr1:g.27549420G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.27549420G>A , CM000663.2:g.27549420G>A	GRCh38
NC_000001.10:g.27875931G>A , CM000663.1:g.27875931G>A	GRCh37
NC_000001.9:g.27748518G>A	NCBI36
NG_034158.1:g.59075C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247087.10:c.2696C>T	ENSP00000247087.4:p.Ala899Val
ENST00000642245.1:c.2696C>T	ENSP00000495072.1:p.Ala899Val
ENST00000642416.1:c.2696C>T	ENSP00000494394.1:p.Ala899Val
ENST00000644989.1:c.2696C>T	ENSP00000495665.1:p.Ala899Val
ENST00000673934.1:c.2696C>T MANE Select	ENSP00000501218.1:p.Ala899Val
ENST00000247087.9:c.2696C>T	ENSP00000247087.4:p.Ala899Val
ENST00000374011.6:c.2696C>T	ENSP00000363123.2:p.Ala899Val
NM_001029882.3:c.2696C>T	NP_001025053.1:p.Ala899Val
XM_005245848.2:c.2696C>T	XP_005245905.1:p.Ala899Val
XM_005245849.2:c.2696C>T	XP_005245906.1:p.Ala899Val
XM_005245850.2:c.2696C>T	XP_005245907.1:p.Ala899Val
XM_005245851.2:c.2696C>T	XP_005245908.1:p.Ala899Val
XM_005245852.2:c.2696C>T	XP_005245909.1:p.Ala899Val
XM_011541255.1:c.2696C>T	XP_011539557.1:p.Ala899Val
XM_011541256.1:c.2696C>T	XP_011539558.1:p.Ala899Val
XM_011541257.1:c.2696C>T	XP_011539559.1:p.Ala899Val
XR_946609.1:n.3653C>T
XM_005245848.3:c.2696C>T	XP_005245905.1:p.Ala899Val
XM_005245849.3:c.2696C>T	XP_005245906.1:p.Ala899Val
XM_005245850.3:c.2696C>T	XP_005245907.1:p.Ala899Val
XM_005245851.3:c.2696C>T	XP_005245908.1:p.Ala899Val
XM_005245852.3:c.2696C>T	XP_005245909.1:p.Ala899Val
XM_011541256.2:c.2696C>T	XP_011539558.1:p.Ala899Val
XM_011541257.2:c.2696C>T	XP_011539559.1:p.Ala899Val
XM_024446461.1:c.2696C>T	XP_024302229.1:p.Ala899Val
XR_946609.2:n.3763C>T
NM_001371928.1:c.2696C>T MANE Select	NP_001358857.1:p.Ala899Val