Canonical Allele Identifier: CA1306196285

Gene: G6PC2 SPC25

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168906638T= , CM000664.2:g.168906638T=	GRCh38
NC_000002.11:g.169763148T= , CM000664.1:g.169763148T=	GRCh37
NC_000002.10:g.169471394T=	NCBI36
NG_011682.1:g.10399T=

Transcript Alleles

HGVS	Amino-acid Change
NM_021176.3:c.441-26T= (G6PC2) MANE Select	NP_066999.1:n.441-26T=
ENST00000375363.8:c.441-26T= (G6PC2) MANE Select	ENSP00000364512.3:n.441-26T=
NM_001081686.1:c.441-930T= (G6PC2)	NP_001075155.1:n.441-930T=
NM_001081686.2:c.441-930T= (G6PC2)	NP_001075155.1:n.441-930T=
NM_021176.2:c.441-26T= (G6PC2)	NP_066999.1:n.441-26T=
ENST00000282075.5:c.*22-26T= (G6PC2)	ENSP00000282075.4:n.*22-26T=
ENST00000375363.7:c.441-26T= (G6PC2)	ENSP00000364512.3:n.441-26T=
ENST00000421979.1:c.219-930T= (G6PC2)	ENSP00000392183.1:n.219-930T=
ENST00000429379.2:c.441-930T= (G6PC2)	ENSP00000396939.2:n.441-930T=
ENST00000451987.5:c.-173+6562A= (SPC25)	ENSP00000393322.1:n.-173+6562A=
ENST00000461586.1:n.157-930T= (G6PC2)
ENST00000472216.2:n.176+6558A= (SPC25)
XM_011511564.1:c.329-930T= (G6PC2)	XP_011509866.1:n.329-930T=
XM_011511564.3:c.329-930T= (G6PC2)	XP_011509866.1:n.329-930T=
XM_011511565.1:c.93-26T= (G6PC2)	XP_011509867.1:n.93-26T=
XM_011511565.3:c.93-26T= (G6PC2)	XP_011509867.1:n.93-26T=