Canonical Allele Identifier: CA2210538768

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134602T= , CM000678.2:g.17134602T=	GRCh38
NC_000016.9:g.17228459T= , CM000678.1:g.17228459T=	GRCh37
NC_000016.8:g.17135960T=	NCBI36
NG_015843.1:g.341280A=
NG_015843.2:g.341280A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1898A= MANE Select	ENSP00000261381.6:p.Asn633=
ENST00000261381.6:c.1898A=	ENSP00000261381.6:p.Asn633=
NM_022166.3:c.1898A=	NP_071449.1:p.Asn633=
XM_011522574.1:c.1898A=	XP_011520876.1:p.Asn633=
XR_933140.1:n.82+52T=
XR_933141.1:n.75+52T=
XR_933143.1:n.82+52T=
NR_135179.1:n.47+52T=
XM_017023539.2:c.1898A=	XP_016879028.1:p.Asn633=
XM_017023540.2:c.1898A=	XP_016879029.1:p.Asn633=
NM_022166.4:c.1898A= MANE Select	NP_071449.1:p.Asn633=