Canonical Allele Identifier: CA913015555

Gene: GCDH

Linked Data

• MyVariant Identifiers: chr19:g.13007016dup (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896202dup , CM000681.2:g.12896202dup	GRCh38
NC_000019.9:g.13007016dup , CM000681.1:g.13007016dup	GRCh37
NC_000019.8:g.12868016dup	NCBI36
NG_009292.1:g.10043dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.636-3dup MANE Select	ENSP00000222214.4:n.636-3dup
ENST00000222214.9:c.636-3dup	ENSP00000222214.4:n.636-3dup
ENST00000421816.6:n.614-3dup
ENST00000585420.5:n.1001-38dup
ENST00000590530.5:c.*76-3dup	ENSP00000468452.1:n.*76-3dup
ENST00000591043.1:n.672-3dup
ENST00000591470.5:c.636-3dup	ENSP00000466845.1:n.636-3dup
NM_000159.3:c.636-3dup	NP_000150.1:n.636-3dup
NM_013976.3:c.636-3dup	NP_039663.1:n.636-3dup
NR_102316.1:n.799-3dup
NR_102317.1:n.1052-38dup
XM_006722721.2:c.636-3dup	XP_006722784.1:n.636-3dup
XM_011527899.1:c.636-3dup	XP_011526201.1:n.636-3dup
XM_011527900.1:c.636-3dup	XP_011526202.1:n.636-3dup
XM_011527899.2:c.636-3dup	XP_011526201.1:n.636-3dup
XM_011527900.2:c.636-3dup	XP_011526202.1:n.636-3dup
XM_017026580.1:c.636-3dup	XP_016882069.1:n.636-3dup
NM_000159.4:c.636-3dup MANE Select	NP_000150.1:n.636-3dup
NM_013976.4:c.636-3dup	NP_039663.1:n.636-3dup
NM_013976.5:c.636-3dup	NP_039663.1:n.636-3dup