Canonical Allele Identifier: CA2631986875

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17134772-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134772A>G , CM000678.2:g.17134772A>G	GRCh38
NC_000016.9:g.17228629A>G , CM000678.1:g.17228629A>G	GRCh37
NC_000016.8:g.17136130A>G	NCBI36
NG_015843.1:g.341110T>C
NG_015843.2:g.341110T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1765-37T>C MANE Select	ENSP00000261381.6:n.1765-37T>C
ENST00000261381.6:c.1765-37T>C	ENSP00000261381.6:n.1765-37T>C
NM_022166.3:c.1765-37T>C	NP_071449.1:n.1765-37T>C
XM_011522574.1:c.1765-37T>C	XP_011520876.1:n.1765-37T>C
XR_933140.1:n.82+222A>G
XR_933141.1:n.75+222A>G
XR_933143.1:n.82+222A>G
NR_135179.1:n.47+222A>G
XM_017023539.2:c.1765-37T>C	XP_016879028.1:n.1765-37T>C
XM_017023540.2:c.1765-37T>C	XP_016879029.1:n.1765-37T>C
NM_022166.4:c.1765-37T>C MANE Select	NP_071449.1:n.1765-37T>C