Canonical Allele Identifier: CA371124711

Gene: HGSNAT

Linked Data

• MyVariant Identifiers: chr8:g.42995755G>C (hg19) ; chr8:g.43140612G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43140612G>C , CM000670.2:g.43140612G>C	GRCh38
NC_000008.10:g.42995755G>C , CM000670.1:g.42995755G>C	GRCh37
NC_000008.9:g.43114912G>C	NCBI36
NG_009552.1:g.5164G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000379644.9:c.116G>C MANE Select	ENSP00000368965.4:p.Arg39Pro
ENST00000379644.8:c.116G>C	ENSP00000368965.4:p.Arg39Pro
ENST00000517319.1:c.116G>C	ENSP00000430032.1:p.Arg39Pro
ENST00000520704.1:c.-35G>C	ENSP00000429109.1:n.-35G>C
NM_152419.2:c.116G>C	NP_689632.2:p.Arg39Pro
XM_005273409.1:c.116G>C	XP_005273466.1:p.Arg39Pro
XM_005273410.1:c.116G>C	XP_005273467.1:p.Arg39Pro
XM_005273411.1:c.116G>C	XP_005273468.1:p.Arg39Pro
XM_005273412.2:c.116G>C	XP_005273469.1:p.Arg39Pro
NM_001363227.1:c.116G>C	NP_001350156.1:p.Arg39Pro
NM_001363228.1:c.116G>C	NP_001350157.1:p.Arg39Pro
NM_001363229.1:c.-718G>C	NP_001350158.1:n.-718G>C
XM_005273412.4:c.116G>C	XP_005273469.1:p.Arg39Pro
NM_152419.3:c.116G>C MANE Select	NP_689632.2:p.Arg39Pro
NM_001363227.2:c.116G>C	NP_001350156.1:p.Arg39Pro
NM_001363228.2:c.116G>C	NP_001350157.1:p.Arg39Pro
NM_001363229.2:c.-718G>C	NP_001350158.1:n.-718G>C