Canonical Allele Identifier: CA397091889
Community Standard Title: NM_000512.5(GALNS):c.155C>T (p.Pro52Leu)
Gene: GALNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88842795G>A , CM000678.2:g.88842795G>A GRCh38
NC_000016.9:g.88909203G>A , CM000678.1:g.88909203G>A GRCh37
NC_000016.8:g.87436704G>A NCBI36
NG_008667.1:g.19172C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000512.5:c.155C>T MANE Select NP_000503.1:p.Pro52Leu
ENST00000268695.10:c.155C>T MANE Select ENSP00000268695.5:p.Pro52Leu
NM_000512.4:c.155C>T NP_000503.1:p.Pro52Leu
NM_001323543.1:c.-311-824C>T NP_001310472.1:n.-311-824C>T
NM_001323543.2:c.-311-824C>T NP_001310472.1:n.-311-824C>T
NM_001323544.1:c.173C>T NP_001310473.1:p.Pro58Leu
NM_001323544.2:c.173C>T NP_001310473.1:p.Pro58Leu
ENST00000268695.9:c.155C>T ENSP00000268695.5:p.Pro52Leu
ENST00000562593.5:n.2830C>T
ENST00000562831.1:c.29-824C>T ENSP00000455174.1:n.29-824C>T
ENST00000565364.1:n.290C>T
ENST00000567525.5:c.70-824C>T ENSP00000454484.1:n.70-824C>T
ENST00000568613.5:c.274C>T ENSP00000457921.1:n.274C>T
XM_005256301.2:c.155C>T XP_005256358.1:p.Pro52Leu
XM_005256301.3:c.155C>T XP_005256358.1:p.Pro52Leu
XM_005256302.1:c.173C>T XP_005256359.1:p.Pro58Leu
XM_011522982.1:c.173C>T XP_011521284.1:p.Pro58Leu
XM_011522982.2:c.173C>T XP_011521284.1:p.Pro58Leu
XM_011522984.1:c.173C>T XP_011521286.1:p.Pro58Leu
XM_017023111.2:c.173C>T XP_016878600.1:p.Pro58Leu
XM_017023112.2:c.173C>T XP_016878601.1:p.Pro58Leu
XM_017023113.1:c.-311-824C>T XP_016878602.1:n.-311-824C>T