Canonical Allele Identifier: CA394875282
Gene: XYLT1 HGNC NCBI

Linked Data

dbSNP Id: rs748613285

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138434T>G , CM000678.2:g.17138434T>G GRCh38
NC_000016.9:g.17232291T>G , CM000678.1:g.17232291T>G GRCh37
NC_000016.8:g.17139792T>G NCBI36
NG_015843.1:g.337448A>C
NG_015843.2:g.337448A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1685A>C MANE Select ENSP00000261381.6:p.Lys562Thr
ENST00000261381.6:c.1685A>C ENSP00000261381.6:p.Lys562Thr
NM_022166.3:c.1685A>C NP_071449.1:p.Lys562Thr
XM_011522574.1:c.1685A>C XP_011520876.1:p.Lys562Thr
XR_933141.1:n.367T>G
NR_135179.1:n.339T>G
XM_017023539.2:c.1685A>C XP_016879028.1:p.Lys562Thr
XM_017023540.2:c.1685A>C XP_016879029.1:p.Lys562Thr
NM_022166.4:c.1685A>C MANE Select NP_071449.1:p.Lys562Thr