Canonical Allele Identifier: CA394875234
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138416A>C , CM000678.2:g.17138416A>C GRCh38
NC_000016.9:g.17232273A>C , CM000678.1:g.17232273A>C GRCh37
NC_000016.8:g.17139774A>C NCBI36
NG_015843.1:g.337466T>G
NG_015843.2:g.337466T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1703T>G MANE Select ENSP00000261381.6:p.Ile568Ser
ENST00000261381.6:c.1703T>G ENSP00000261381.6:p.Ile568Ser
NM_022166.3:c.1703T>G NP_071449.1:p.Ile568Ser
XM_011522574.1:c.1703T>G XP_011520876.1:p.Ile568Ser
XR_933141.1:n.349A>C
NR_135179.1:n.321A>C
XM_017023539.2:c.1703T>G XP_016879028.1:p.Ile568Ser
XM_017023540.2:c.1703T>G XP_016879029.1:p.Ile568Ser
NM_022166.4:c.1703T>G MANE Select NP_071449.1:p.Ile568Ser