Canonical Allele Identifier: CA395219800
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17134710G>C , CM000678.2:g.17134710G>C GRCh38
NC_000016.9:g.17228567G>C , CM000678.1:g.17228567G>C GRCh37
NC_000016.8:g.17136068G>C NCBI36
NG_015843.1:g.341172C>G
NG_015843.2:g.341172C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1790C>G MANE Select ENSP00000261381.6:p.Ala597Gly
ENST00000261381.6:c.1790C>G ENSP00000261381.6:p.Ala597Gly
NM_022166.3:c.1790C>G NP_071449.1:p.Ala597Gly
XM_011522574.1:c.1790C>G XP_011520876.1:p.Ala597Gly
XR_933140.1:n.82+160G>C
XR_933141.1:n.75+160G>C
XR_933143.1:n.82+160G>C
NR_135179.1:n.47+160G>C
XM_017023539.2:c.1790C>G XP_016879028.1:p.Ala597Gly
XM_017023540.2:c.1790C>G XP_016879029.1:p.Ala597Gly
NM_022166.4:c.1790C>G MANE Select NP_071449.1:p.Ala597Gly