Canonical Allele Identifier: CA7927482
Community Standard Title: NM_022166.4(XYLT1):c.2768G>A (p.Gly923Asp)
Gene: XYLT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17108807C>T , CM000678.2:g.17108807C>T GRCh38
NC_000016.9:g.17202664C>T , CM000678.1:g.17202664C>T GRCh37
NC_000016.8:g.17110165C>T NCBI36
NG_015843.1:g.367075G>A
NG_015843.2:g.367075G>A

Transcript Alleles

HGVS Amino-acid Change
NM_022166.4:c.2768G>A MANE Select NP_071449.1:p.Gly923Asp
ENST00000261381.7:c.2768G>A MANE Select ENSP00000261381.6:p.Gly923Asp
NM_022166.3:c.2768G>A NP_071449.1:p.Gly923Asp
ENST00000261381.6:c.2768G>A ENSP00000261381.6:p.Gly923Asp
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