Canonical Allele Identifier: CA1304213806

Gene: GRB14

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.164581720G= , CM000664.2:g.164581720G=	GRCh38
NC_000002.11:g.165438230G= , CM000664.1:g.165438230G=	GRCh37
NC_000002.10:g.165146476G=	NCBI36
NG_052839.1:g.45131C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263915.8:c.325-33904C= MANE Select	ENSP00000263915.3:n.325-33904C=
ENST00000263915.7:c.325-33904C=	ENSP00000263915.3:n.325-33904C=
ENST00000424693.1:c.151-33904C=	ENSP00000401702.1:n.151-33904C=
ENST00000446413.6:c.190-33904C=	ENSP00000416786.2:n.190-33904C=
ENST00000488342.5:n.408-33904C=
NM_004490.2:c.325-33904C=	NP_004481.2:n.325-33904C=
XM_011511022.1:c.325-33904C=	XP_011509324.1:n.325-33904C=
XR_427085.2:n.494-33904C=
XM_011511022.2:c.325-33904C=	XP_011509324.1:n.325-33904C=
XM_024452815.1:c.103-33904C=	XP_024308583.1:n.103-33904C=
XM_024452816.1:c.103-33904C=	XP_024308584.1:n.103-33904C=
XR_427085.3:n.498-33904C=
NM_004490.3:c.325-33904C= MANE Select	NP_004481.2:n.325-33904C=