Canonical Allele Identifier: CA394875258
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138425T>A , CM000678.2:g.17138425T>A GRCh38
NC_000016.9:g.17232282T>A , CM000678.1:g.17232282T>A GRCh37
NC_000016.8:g.17139783T>A NCBI36
NG_015843.1:g.337457A>T
NG_015843.2:g.337457A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1694A>T MANE Select ENSP00000261381.6:p.Tyr565Phe
ENST00000261381.6:c.1694A>T ENSP00000261381.6:p.Tyr565Phe
NM_022166.3:c.1694A>T NP_071449.1:p.Tyr565Phe
XM_011522574.1:c.1694A>T XP_011520876.1:p.Tyr565Phe
XR_933141.1:n.358T>A
NR_135179.1:n.330T>A
XM_017023539.2:c.1694A>T XP_016879028.1:p.Tyr565Phe
XM_017023540.2:c.1694A>T XP_016879029.1:p.Tyr565Phe
NM_022166.4:c.1694A>T MANE Select NP_071449.1:p.Tyr565Phe