Canonical Allele Identifier: CA494104104

Gene: XYLT1

Linked Data

• MyVariant Identifiers: chr16:g.17228566G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134709G>C , CM000678.2:g.17134709G>C	GRCh38
NC_000016.9:g.17228566G>C , CM000678.1:g.17228566G>C	GRCh37
NC_000016.8:g.17136067G>C	NCBI36
NG_015843.1:g.341173C>G
NG_015843.2:g.341173C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261381.7:c.1791C>G MANE Select	ENSP00000261381.6:p.Ala597=
ENST00000261381.6:c.1791C>G	ENSP00000261381.6:p.Ala597=
NM_022166.3:c.1791C>G	NP_071449.1:p.Ala597=
XM_011522574.1:c.1791C>G	XP_011520876.1:p.Ala597=
XR_933140.1:n.82+159G>C
XR_933141.1:n.75+159G>C
XR_933143.1:n.82+159G>C
NR_135179.1:n.47+159G>C
XM_017023539.2:c.1791C>G	XP_016879028.1:p.Ala597=
XM_017023540.2:c.1791C>G	XP_016879029.1:p.Ala597=
NM_022166.4:c.1791C>G MANE Select	NP_071449.1:p.Ala597=