Canonical Allele Identifier: CA493798252

Gene: XYLT1

Linked Data

• dbSNP Id: rs746009558
• gnomAD v2: 16-17232396-G-C
• gnomAD v4: 16-17138539-G-C
• MyVariant Identifiers: chr16:g.17232396G>C (hg19) ; chr16:g.17138539G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138539G>C , CM000678.2:g.17138539G>C	GRCh38
NC_000016.9:g.17232396G>C , CM000678.1:g.17232396G>C	GRCh37
NC_000016.8:g.17139897G>C	NCBI36
NG_015843.1:g.337343C>G
NG_015843.2:g.337343C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261381.7:c.1588-8C>G MANE Select	ENSP00000261381.6:n.1588-8C>G
ENST00000261381.6:c.1588-8C>G	ENSP00000261381.6:n.1588-8C>G
NM_022166.3:c.1588-8C>G	NP_071449.1:n.1588-8C>G
XM_011522574.1:c.1588-8C>G	XP_011520876.1:n.1588-8C>G
XR_933141.1:n.472G>C
NR_135179.1:n.444G>C
XM_017023539.2:c.1588-8C>G	XP_016879028.1:n.1588-8C>G
XM_017023540.2:c.1588-8C>G	XP_016879029.1:n.1588-8C>G
NM_022166.4:c.1588-8C>G MANE Select	NP_071449.1:n.1588-8C>G