Canonical Allele Identifier: CA1304177517

Gene: GRB14

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.164497202C= , CM000664.2:g.164497202C=	GRCh38
NC_000002.11:g.165353712C= , CM000664.1:g.165353712C=	GRCh37
NC_000002.10:g.165061958C=	NCBI36
NG_052839.1:g.129649G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696453.2:c.1033+9G=	ENSP00000512640.1:n.1033+9G=
ENST00000263915.8:c.1294+9G= MANE Select	ENSP00000263915.3:n.1294+9G=
ENST00000263915.7:c.1294+9G=	ENSP00000263915.3:n.1294+9G=
ENST00000446413.6:c.1159+9G=	ENSP00000416786.2:n.1159+9G=
ENST00000488342.5:n.1430+9G=
NM_001303422.1:c.1033+9G=	NP_001290351.1:n.1033+9G=
NM_004490.2:c.1294+9G=	NP_004481.2:n.1294+9G=
XM_006712457.2:c.694+9G=	XP_006712520.1:n.694+9G=
XM_017003899.1:c.694+9G=	XP_016859388.1:n.694+9G=
XM_024452815.1:c.1072+9G=	XP_024308583.1:n.1072+9G=
XM_024452816.1:c.1072+9G=	XP_024308584.1:n.1072+9G=
NM_001303422.2:c.1033+9G=	NP_001290351.1:n.1033+9G=
NM_004490.3:c.1294+9G= MANE Select	NP_004481.2:n.1294+9G=