Canonical Allele Identifier: CA397083306

Gene: GALNS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88837721A>C , CM000678.2:g.88837721A>C	GRCh38
NC_000016.9:g.88904129A>C , CM000678.1:g.88904129A>C	GRCh37
NC_000016.8:g.87431630A>C	NCBI36
NG_008667.1:g.24246T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000512.5:c.467T>G MANE Select	NP_000503.1:p.Phe156Cys
ENST00000268695.10:c.467T>G MANE Select	ENSP00000268695.5:p.Phe156Cys
NM_000512.4:c.467T>G	NP_000503.1:p.Phe156Cys
NM_001323543.1:c.-89T>G	NP_001310472.1:n.-89T>G
NM_001323543.2:c.-89T>G	NP_001310472.1:n.-89T>G
NM_001323544.1:c.485T>G	NP_001310473.1:p.Phe162Cys
NM_001323544.2:c.485T>G	NP_001310473.1:p.Phe162Cys
ENST00000268695.9:c.467T>G	ENSP00000268695.5:p.Phe156Cys
ENST00000561812.1:n.423T>G
ENST00000562593.5:n.3876T>G
ENST00000562831.1:c.251T>G	ENSP00000455174.1:p.Phe84Cys
ENST00000562931.5:n.55T>G
ENST00000566563.1:n.169T>G
ENST00000567525.5:c.248-1454T>G	ENSP00000454484.1:n.248-1454T>G
ENST00000568613.5:c.586T>G	ENSP00000457921.1:n.586T>G
XM_005256301.2:c.467T>G	XP_005256358.1:p.Phe156Cys
XM_005256301.3:c.467T>G	XP_005256358.1:p.Phe156Cys
XM_005256302.1:c.485T>G	XP_005256359.1:p.Phe162Cys
XM_011522982.1:c.485T>G	XP_011521284.1:p.Phe162Cys
XM_011522982.2:c.485T>G	XP_011521284.1:p.Phe162Cys
XM_011522984.1:c.485T>G	XP_011521286.1:p.Phe162Cys
XM_017023111.2:c.485T>G	XP_016878600.1:p.Phe162Cys
XM_017023112.2:c.485T>G	XP_016878601.1:p.Phe162Cys
XM_017023113.1:c.-89T>G	XP_016878602.1:n.-89T>G