Canonical Allele Identifier: CA8235038
Community Standard Title: NM_000512.5(GALNS):c.641T>C (p.Leu214Pro)
Gene: GALNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88835842A>G , CM000678.2:g.88835842A>G GRCh38
NC_000016.9:g.88902250A>G , CM000678.1:g.88902250A>G GRCh37
NC_000016.8:g.87429751A>G NCBI36
NG_008667.1:g.26125T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000512.5:c.641T>C MANE Select NP_000503.1:p.Leu214Pro
ENST00000268695.10:c.641T>C MANE Select ENSP00000268695.5:p.Leu214Pro
NM_000512.4:c.641T>C NP_000503.1:p.Leu214Pro
NM_001323543.1:c.86T>C NP_001310472.1:p.Leu29Pro
NM_001323543.2:c.86T>C NP_001310472.1:p.Leu29Pro
NM_001323544.1:c.659T>C NP_001310473.1:p.Leu220Pro
NM_001323544.2:c.659T>C NP_001310473.1:p.Leu220Pro
ENST00000268695.9:c.641T>C ENSP00000268695.5:p.Leu214Pro
ENST00000562593.5:n.4050T>C
ENST00000562831.1:c.425T>C ENSP00000455174.1:p.Leu142Pro
ENST00000562931.5:n.229T>C
ENST00000566563.1:n.343T>C
ENST00000567525.5:c.322T>C ENSP00000454484.1:n.322T>C
ENST00000568613.5:c.760T>C ENSP00000457921.1:n.760T>C
XM_005256301.2:c.641T>C XP_005256358.1:p.Leu214Pro
XM_005256301.3:c.641T>C XP_005256358.1:p.Leu214Pro
XM_005256302.1:c.659T>C XP_005256359.1:p.Leu220Pro
XM_011522982.1:c.659T>C XP_011521284.1:p.Leu220Pro
XM_011522982.2:c.659T>C XP_011521284.1:p.Leu220Pro
XM_011522984.1:c.659T>C XP_011521286.1:p.Leu220Pro
XM_017023111.2:c.659T>C XP_016878600.1:p.Leu220Pro
XM_017023112.2:c.659T>C XP_016878601.1:p.Leu220Pro
XM_017023113.1:c.86T>C XP_016878602.1:p.Leu29Pro