Canonical Allele Identifier: CA494104114

Gene: XYLT1

Linked Data

• dbSNP Id: rs1334593668
• MyVariant Identifiers: chr16:g.17228569A>G (hg19) ; chr16:g.17134712A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134712A>G , CM000678.2:g.17134712A>G	GRCh38
NC_000016.9:g.17228569A>G , CM000678.1:g.17228569A>G	GRCh37
NC_000016.8:g.17136070A>G	NCBI36
NG_015843.1:g.341170T>C
NG_015843.2:g.341170T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1788T>C MANE Select	ENSP00000261381.6:p.Phe596=
ENST00000261381.6:c.1788T>C	ENSP00000261381.6:p.Phe596=
NM_022166.3:c.1788T>C	NP_071449.1:p.Phe596=
XM_011522574.1:c.1788T>C	XP_011520876.1:p.Phe596=
XR_933140.1:n.82+162A>G
XR_933141.1:n.75+162A>G
XR_933143.1:n.82+162A>G
NR_135179.1:n.47+162A>G
XM_017023539.2:c.1788T>C	XP_016879028.1:p.Phe596=
XM_017023540.2:c.1788T>C	XP_016879029.1:p.Phe596=
NM_022166.4:c.1788T>C MANE Select	NP_071449.1:p.Phe596=