Canonical Allele Identifier: CA497080141

Gene: GALNS

Linked Data

• MyVariant Identifiers: chr16:g.88908369T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88841961T>A , CM000678.2:g.88841961T>A	GRCh38
NC_000016.9:g.88908369T>A , CM000678.1:g.88908369T>A	GRCh37
NC_000016.8:g.87435870T>A	NCBI36
NG_008667.1:g.20006A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000268695.10:c.255A>T MANE Select	ENSP00000268695.5:p.Ala85=
ENST00000268695.9:c.255A>T	ENSP00000268695.5:p.Ala85=
ENST00000562593.5:n.3664A>T
ENST00000562831.1:c.39A>T	ENSP00000455174.1:p.Ala13=
ENST00000565364.1:n.390A>T
ENST00000567525.5:c.80A>T	ENSP00000454484.1:p.His27Leu
ENST00000567779.1:n.85A>T
ENST00000568613.5:c.374A>T	ENSP00000457921.1:n.374A>T
NM_000512.4:c.255A>T	NP_000503.1:p.Ala85=
XM_005256301.2:c.255A>T	XP_005256358.1:p.Ala85=
XM_005256302.1:c.273A>T	XP_005256359.1:p.Ala91=
XM_011522982.1:c.273A>T	XP_011521284.1:p.Ala91=
XM_011522984.1:c.273A>T	XP_011521286.1:p.Ala91=
NM_001323543.1:c.-301A>T	NP_001310472.1:n.-301A>T
NM_001323544.1:c.273A>T	NP_001310473.1:p.Ala91=
XM_005256301.3:c.255A>T	XP_005256358.1:p.Ala85=
XM_011522982.2:c.273A>T	XP_011521284.1:p.Ala91=
XM_017023111.2:c.273A>T	XP_016878600.1:p.Ala91=
XM_017023112.2:c.273A>T	XP_016878601.1:p.Ala91=
XM_017023113.1:c.-301A>T	XP_016878602.1:n.-301A>T
NM_000512.5:c.255A>T MANE Select	NP_000503.1:p.Ala85=
NM_001323543.2:c.-301A>T	NP_001310472.1:n.-301A>T
NM_001323544.2:c.273A>T	NP_001310473.1:p.Ala91=