Canonical Allele Identifier: CA11299329
Gene: GALNT14 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1862981

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31074658T>G , CM000664.2:g.31074658T>G GRCh38
NC_000002.10:g.31151028T>G NCBI36
NC_000002.11:g.31297524T>G , CM000664.1:g.31297524T>G GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000324589.9:c.314+40085A>C ENSP00000314500.5:p.=
ENST00000349752.9:c.129+63300A>C ENSP00000288988.6:p.=
ENST00000406653.5:c.69+40085A>C ENSP00000385435.1:p.=
ENST00000424136.5:n.181+57972A>C
ENST00000430167.1:c.129+63300A>C ENSP00000406399.1:p.=
ENST00000455477.5:n.198+50496A>C
ENST00000461193.5:n.164+50496A>C
ENST00000464038.5:n.388+72264A>C
ENST00000485468.1:n.290+4276A>C
ENST00000490212.5:n.364+54619A>C
ENST00000496397.5:n.202-1483A>C
ENST00000498206.5:n.358+40085A>C
NM_001253826.1:c.314+40085A>C NP_001240755.1:p.=
NM_001253827.1:c.69+40085A>C NP_001240756.1:p.=
NM_024572.3:c.129+63300A>C NP_078848.2:p.=
NR_045602.1:n.902+4276A>C
XM_011533104.1:c.447+4276A>C XP_011531406.1:p.=
XM_011533105.1:c.69+40085A>C XP_011531407.1:p.=
XM_011533106.1:c.42+72264A>C XP_011531408.1:p.=