Canonical Allele Identifier: CA494103458

Gene: XYLT1

Linked Data

• COSMIC: COSM6078276
• MyVariant Identifiers: chr16:g.17228362C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134505C>A , CM000678.2:g.17134505C>A	GRCh38
NC_000016.9:g.17228362C>A , CM000678.1:g.17228362C>A	GRCh37
NC_000016.8:g.17135863C>A	NCBI36
NG_015843.1:g.341377G>T
NG_015843.2:g.341377G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1995G>T MANE Select	ENSP00000261381.6:p.Thr665=
ENST00000261381.6:c.1995G>T	ENSP00000261381.6:p.Thr665=
NM_022166.3:c.1995G>T	NP_071449.1:p.Thr665=
XM_011522574.1:c.1995G>T	XP_011520876.1:p.Thr665=
XR_933140.1:n.37C>A
XR_933141.1:n.30C>A
XR_933143.1:n.37C>A
NR_135179.1:n.2C>A
XM_017023539.2:c.1995G>T	XP_016879028.1:p.Thr665=
XM_017023540.2:c.1995G>T	XP_016879029.1:p.Thr665=
NM_022166.4:c.1995G>T MANE Select	NP_071449.1:p.Thr665=