Canonical Allele Identifier: CA2695228345

Gene: GCDH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896266dup , CM000681.2:g.12896266dup	GRCh38
NC_000019.9:g.13007080dup , CM000681.1:g.13007080dup	GRCh37
NC_000019.8:g.12868080dup	NCBI36
NG_009292.1:g.10107dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.697dup MANE Select	ENSP00000222214.4:p.Ile233AsnfsTer?
ENST00000222214.9:c.697dup	ENSP00000222214.4:p.Ile233AsnfsTer?
ENST00000421816.6:n.675dup
ENST00000585420.5:n.1027dup
ENST00000590530.5:c.*137dup	ENSP00000468452.1:n.*137dup
ENST00000591043.1:n.733dup
ENST00000591470.5:c.697dup	ENSP00000466845.1:p.Ile233AsnfsTer?
NM_000159.3:c.697dup	NP_000150.1:p.Ile233AsnfsTer?
NM_013976.3:c.697dup	NP_039663.1:p.Ile233AsnfsTer?
NR_102316.1:n.860dup
NR_102317.1:n.1078dup
XM_006722721.2:c.697dup	XP_006722784.1:p.Ile233AsnfsTer?
XM_011527899.1:c.697dup	XP_011526201.1:p.Ile233AsnfsTer?
XM_011527900.1:c.697dup	XP_011526202.1:p.Ile233AsnfsTer?
XM_011527899.2:c.697dup	XP_011526201.1:p.Ile233AsnfsTer?
XM_011527900.2:c.697dup	XP_011526202.1:p.Ile233AsnfsTer?
XM_017026580.1:c.697dup	XP_016882069.1:p.Ile233AsnfsTer?
NM_000159.4:c.697dup MANE Select	NP_000150.1:p.Ile233AsnfsTer?
NM_013976.4:c.697dup	NP_039663.1:p.Ile233AsnfsTer?
NM_013976.5:c.697dup	NP_039663.1:p.Ile233AsnfsTer?