Canonical Allele Identifier: CA1592684881
Gene: GALNT10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154227774T= , CM000667.2:g.154227774T= GRCh38
NC_000005.9:g.153607334T= , CM000667.1:g.153607334T= GRCh37
NC_000005.8:g.153587527T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000297107.11:c.159+36749T= MANE Select ENSP00000297107.6:n.159+36749T=
ENST00000297107.10:c.159+36749T= ENSP00000297107.6:n.159+36749T=
ENST00000377661.2:c.159+36749T= ENSP00000366889.2:n.159+36749T=
ENST00000425427.6:c.159+36749T= ENSP00000415210.2:n.159+36749T=
ENST00000520647.5:c.159+36749T= ENSP00000428573.1:n.159+36749T=
ENST00000521781.5:n.150+9625T=
NM_198321.3:c.159+36749T= NP_938080.1:n.159+36749T=
NM_198321.4:c.159+36749T= MANE Select NP_938080.1:n.159+36749T=
Search 100 bp 5'
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