Canonical Allele Identifier: CA505778826

Gene: GCDH

Linked Data

• MyVariant Identifiers: chr19:g.13007031G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12896217G>T , CM000681.2:g.12896217G>T	GRCh38
NC_000019.9:g.13007031G>T , CM000681.1:g.13007031G>T	GRCh37
NC_000019.8:g.12868031G>T	NCBI36
NG_009292.1:g.10058G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222214.10:c.648G>T MANE Select	ENSP00000222214.4:p.Ser216=
ENST00000222214.9:c.648G>T	ENSP00000222214.4:p.Ser216=
ENST00000421816.6:n.626G>T
ENST00000585420.5:n.1001-23G>T
ENST00000590530.5:c.*88G>T	ENSP00000468452.1:n.*88G>T
ENST00000591043.1:n.684G>T
ENST00000591470.5:c.648G>T	ENSP00000466845.1:p.Ser216=
NM_000159.3:c.648G>T	NP_000150.1:p.Ser216=
NM_013976.3:c.648G>T	NP_039663.1:p.Ser216=
NR_102316.1:n.811G>T
NR_102317.1:n.1052-23G>T
XM_006722721.2:c.648G>T	XP_006722784.1:p.Ser216=
XM_011527899.1:c.648G>T	XP_011526201.1:p.Ser216=
XM_011527900.1:c.648G>T	XP_011526202.1:p.Ser216=
XM_011527899.2:c.648G>T	XP_011526201.1:p.Ser216=
XM_011527900.2:c.648G>T	XP_011526202.1:p.Ser216=
XM_017026580.1:c.648G>T	XP_016882069.1:p.Ser216=
NM_000159.4:c.648G>T MANE Select	NP_000150.1:p.Ser216=
NM_013976.4:c.648G>T	NP_039663.1:p.Ser216=
NM_013976.5:c.648G>T	NP_039663.1:p.Ser216=