Canonical Allele Identifier: CA4736435

Gene: HGSNAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43146964A>T , CM000670.2:g.43146964A>T	GRCh38
NC_000008.10:g.43002107A>T , CM000670.1:g.43002107A>T	GRCh37
NC_000008.9:g.43121264A>T	NCBI36
NG_009552.1:g.11516A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_152419.3:c.135A>T MANE Select	NP_689632.2:p.Arg45Ser
ENST00000379644.9:c.135A>T MANE Select	ENSP00000368965.4:p.Arg45Ser
NM_001363227.1:c.135A>T	NP_001350156.1:p.Arg45Ser
NM_001363227.2:c.135A>T	NP_001350156.1:p.Arg45Ser
NM_001363228.1:c.135A>T	NP_001350157.1:p.Arg45Ser
NM_001363228.2:c.135A>T	NP_001350157.1:p.Arg45Ser
NM_001363229.1:c.-699A>T	NP_001350158.1:n.-699A>T
NM_001363229.2:c.-699A>T	NP_001350158.1:n.-699A>T
NM_152419.2:c.135A>T	NP_689632.2:p.Arg45Ser
ENST00000379644.8:c.135A>T	ENSP00000368965.4:p.Arg45Ser
ENST00000517319.1:c.135A>T	ENSP00000430032.1:p.Arg45Ser
ENST00000520704.1:c.-16A>T	ENSP00000429109.1:n.-16A>T
XM_005273409.1:c.135A>T	XP_005273466.1:p.Arg45Ser
XM_005273410.1:c.135A>T	XP_005273467.1:p.Arg45Ser
XM_005273411.1:c.135A>T	XP_005273468.1:p.Arg45Ser
XM_005273412.2:c.135A>T	XP_005273469.1:p.Arg45Ser
XM_005273412.4:c.135A>T	XP_005273469.1:p.Arg45Ser