Canonical Allele Identifier: CA455449427

Gene: GUSB

Linked Data

• MyVariant Identifiers: chr7:g.65447141C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65982154C>A , CM000669.2:g.65982154C>A	GRCh38
NC_000007.13:g.65447141C>A , CM000669.1:g.65447141C>A	GRCh37
NC_000007.12:g.65084576C>A	NCBI36
NG_016197.1:g.5161G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.30G>T MANE Select	ENSP00000302728.4:p.Ala10=
ENST00000304895.8:c.30G>T	ENSP00000302728.4:p.Ala10=
ENST00000421103.5:c.30G>T	ENSP00000391390.1:p.Ala10=
ENST00000430730.5:c.30G>T	ENSP00000411859.1:p.Ala10=
ENST00000446111.1:c.30G>T	ENSP00000416793.1:p.Ala10=
ENST00000447929.5:c.30G>T	ENSP00000411262.1:p.Ala10=
NM_000181.3:c.30G>T	NP_000172.2:p.Ala10=
NM_001284290.1:c.30G>T	NP_001271219.1:p.Ala10=
NM_001293104.1:c.-356G>T	NP_001280033.1:n.-356G>T
NM_001293105.1:c.-300G>T	NP_001280034.1:n.-300G>T
NR_120531.1:n.161G>T
XM_005250297.3:c.30G>T	XP_005250354.1:p.Ala10=
XM_011516113.1:c.-300G>T	XP_011514415.1:n.-300G>T
XR_927461.1:n.156G>T
XM_005250297.4:c.30G>T	XP_005250354.1:p.Ala10=
XM_011516114.2:c.-656G>T	XP_011514416.1:n.-656G>T
XM_017012091.1:c.-300G>T	XP_016867580.1:n.-300G>T
XM_017012092.1:c.-356G>T	XP_016867581.1:n.-356G>T
XM_017012093.2:c.-656G>T	XP_016867582.1:n.-656G>T
XR_001744658.2:n.75G>T
XR_001744659.2:n.75G>T
XR_001744660.2:n.75G>T
XR_001744661.2:n.75G>T
XR_927461.3:n.75G>T
NM_000181.4:c.30G>T MANE Select	NP_000172.2:p.Ala10=
NM_001284290.2:c.30G>T	NP_001271219.1:p.Ala10=
NM_001293104.2:c.-356G>T	NP_001280033.1:n.-356G>T
NM_001293105.2:c.-300G>T	NP_001280034.1:n.-300G>T
NR_120531.2:n.60G>T