Canonical Allele Identifier: CA367655520

Gene: GUSB

Linked Data

• gnomAD v4: 7-65982126-C-A
• MyVariant Identifiers: chr7:g.65447113C>A (hg19) ; chr7:g.65982126C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65982126C>A , CM000669.2:g.65982126C>A	GRCh38
NC_000007.13:g.65447113C>A , CM000669.1:g.65447113C>A	GRCh37
NC_000007.12:g.65084548C>A	NCBI36
NG_016197.1:g.5189G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.58G>T MANE Select	ENSP00000302728.4:p.Ala20Ser
ENST00000304895.8:c.58G>T	ENSP00000302728.4:p.Ala20Ser
ENST00000421103.5:c.58G>T	ENSP00000391390.1:p.Ala20Ser
ENST00000430730.5:c.58G>T	ENSP00000411859.1:p.Ala20Ser
ENST00000446111.1:c.58G>T	ENSP00000416793.1:p.Ala20Ser
ENST00000447929.5:c.58G>T	ENSP00000411262.1:p.Ala20Ser
NM_000181.3:c.58G>T	NP_000172.2:p.Ala20Ser
NM_001284290.1:c.58G>T	NP_001271219.1:p.Ala20Ser
NM_001293104.1:c.-328G>T	NP_001280033.1:n.-328G>T
NM_001293105.1:c.-272G>T	NP_001280034.1:n.-272G>T
NR_120531.1:n.189G>T
XM_005250297.3:c.58G>T	XP_005250354.1:p.Ala20Ser
XM_011516113.1:c.-272G>T	XP_011514415.1:n.-272G>T
XR_927461.1:n.184G>T
XM_005250297.4:c.58G>T	XP_005250354.1:p.Ala20Ser
XM_011516114.2:c.-628G>T	XP_011514416.1:n.-628G>T
XM_017012091.1:c.-272G>T	XP_016867580.1:n.-272G>T
XM_017012092.1:c.-328G>T	XP_016867581.1:n.-328G>T
XM_017012093.2:c.-628G>T	XP_016867582.1:n.-628G>T
XR_001744658.2:n.103G>T
XR_001744659.2:n.103G>T
XR_001744660.2:n.103G>T
XR_001744661.2:n.103G>T
XR_927461.3:n.103G>T
NM_000181.4:c.58G>T MANE Select	NP_000172.2:p.Ala20Ser
NM_001284290.2:c.58G>T	NP_001271219.1:p.Ala20Ser
NM_001293104.2:c.-328G>T	NP_001280033.1:n.-328G>T
NM_001293105.2:c.-272G>T	NP_001280034.1:n.-272G>T
NR_120531.2:n.88G>T