Canonical Allele Identifier: CA367655684

Gene: GUSB

Linked Data

• gnomAD v4: 7-65982155-G-A
• MyVariant Identifiers: chr7:g.65447142G>A (hg19) ; chr7:g.65982155G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65982155G>A , CM000669.2:g.65982155G>A	GRCh38
NC_000007.13:g.65447142G>A , CM000669.1:g.65447142G>A	GRCh37
NC_000007.12:g.65084577G>A	NCBI36
NG_016197.1:g.5160C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.29C>T MANE Select	ENSP00000302728.4:p.Ala10Val
ENST00000304895.8:c.29C>T	ENSP00000302728.4:p.Ala10Val
ENST00000421103.5:c.29C>T	ENSP00000391390.1:p.Ala10Val
ENST00000430730.5:c.29C>T	ENSP00000411859.1:p.Ala10Val
ENST00000446111.1:c.29C>T	ENSP00000416793.1:p.Ala10Val
ENST00000447929.5:c.29C>T	ENSP00000411262.1:p.Ala10Val
NM_000181.3:c.29C>T	NP_000172.2:p.Ala10Val
NM_001284290.1:c.29C>T	NP_001271219.1:p.Ala10Val
NM_001293104.1:c.-357C>T	NP_001280033.1:n.-357C>T
NM_001293105.1:c.-301C>T	NP_001280034.1:n.-301C>T
NR_120531.1:n.160C>T
XM_005250297.3:c.29C>T	XP_005250354.1:p.Ala10Val
XM_011516113.1:c.-301C>T	XP_011514415.1:n.-301C>T
XR_927461.1:n.155C>T
XM_005250297.4:c.29C>T	XP_005250354.1:p.Ala10Val
XM_011516114.2:c.-657C>T	XP_011514416.1:n.-657C>T
XM_017012091.1:c.-301C>T	XP_016867580.1:n.-301C>T
XM_017012092.1:c.-357C>T	XP_016867581.1:n.-357C>T
XM_017012093.2:c.-657C>T	XP_016867582.1:n.-657C>T
XR_001744658.2:n.74C>T
XR_001744659.2:n.74C>T
XR_001744660.2:n.74C>T
XR_001744661.2:n.74C>T
XR_927461.3:n.74C>T
NM_000181.4:c.29C>T MANE Select	NP_000172.2:p.Ala10Val
NM_001284290.2:c.29C>T	NP_001271219.1:p.Ala10Val
NM_001293104.2:c.-357C>T	NP_001280033.1:n.-357C>T
NM_001293105.2:c.-301C>T	NP_001280034.1:n.-301C>T
NR_120531.2:n.59C>T