Canonical Allele Identifier: CA397091125
Community Standard Title: NM_000512.5(GALNS):c.242C>T (p.Pro81Leu)
Gene: GALNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88842708G>A , CM000678.2:g.88842708G>A GRCh38
NC_000016.9:g.88909116G>A , CM000678.1:g.88909116G>A GRCh37
NC_000016.8:g.87436617G>A NCBI36
NG_008667.1:g.19259C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000512.5:c.242C>T MANE Select NP_000503.1:p.Pro81Leu
ENST00000268695.10:c.242C>T MANE Select ENSP00000268695.5:p.Pro81Leu
NM_000512.4:c.242C>T NP_000503.1:p.Pro81Leu
NM_001323543.1:c.-311-737C>T NP_001310472.1:n.-311-737C>T
NM_001323543.2:c.-311-737C>T NP_001310472.1:n.-311-737C>T
NM_001323544.1:c.260C>T NP_001310473.1:p.Pro87Leu
NM_001323544.2:c.260C>T NP_001310473.1:p.Pro87Leu
ENST00000268695.9:c.242C>T ENSP00000268695.5:p.Pro81Leu
ENST00000562593.5:n.2917C>T
ENST00000562831.1:c.29-737C>T ENSP00000455174.1:n.29-737C>T
ENST00000565364.1:n.377C>T
ENST00000567525.5:c.70-737C>T ENSP00000454484.1:n.70-737C>T
ENST00000568613.5:c.361C>T ENSP00000457921.1:n.361C>T
XM_005256301.2:c.242C>T XP_005256358.1:p.Pro81Leu
XM_005256301.3:c.242C>T XP_005256358.1:p.Pro81Leu
XM_005256302.1:c.260C>T XP_005256359.1:p.Pro87Leu
XM_011522982.1:c.260C>T XP_011521284.1:p.Pro87Leu
XM_011522982.2:c.260C>T XP_011521284.1:p.Pro87Leu
XM_011522984.1:c.260C>T XP_011521286.1:p.Pro87Leu
XM_017023111.2:c.260C>T XP_016878600.1:p.Pro87Leu
XM_017023112.2:c.260C>T XP_016878601.1:p.Pro87Leu
XM_017023113.1:c.-311-737C>T XP_016878602.1:n.-311-737C>T