Canonical Allele Identifier: CA394875291

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138438-A-C
• MyVariant Identifiers: chr16:g.17232295A>C (hg19) ; chr16:g.17138438A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138438A>C , CM000678.2:g.17138438A>C	GRCh38
NC_000016.9:g.17232295A>C , CM000678.1:g.17232295A>C	GRCh37
NC_000016.8:g.17139796A>C	NCBI36
NG_015843.1:g.337444T>G
NG_015843.2:g.337444T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261381.7:c.1681T>G MANE Select	ENSP00000261381.6:p.Cys561Gly
ENST00000261381.6:c.1681T>G	ENSP00000261381.6:p.Cys561Gly
NM_022166.3:c.1681T>G	NP_071449.1:p.Cys561Gly
XM_011522574.1:c.1681T>G	XP_011520876.1:p.Cys561Gly
XR_933141.1:n.371A>C
NR_135179.1:n.343A>C
XM_017023539.2:c.1681T>G	XP_016879028.1:p.Cys561Gly
XM_017023540.2:c.1681T>G	XP_016879029.1:p.Cys561Gly
NM_022166.4:c.1681T>G MANE Select	NP_071449.1:p.Cys561Gly