Canonical Allele Identifier: CA2631987474

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138225-T-TTC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138226_17138227insCT , CM000678.2:g.17138226_17138227insCT	GRCh38
NC_000016.9:g.17232083_17232084insCT , CM000678.1:g.17232083_17232084insCT	GRCh37
NC_000016.8:g.17139584_17139585insCT	NCBI36
NG_015843.1:g.337656_337657insGA
NG_015843.2:g.337656_337657insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+129_1764+130insGA MANE Select	ENSP00000261381.6:n.1764+129_1764+130insGA
ENST00000261381.6:c.1764+129_1764+130insGA	ENSP00000261381.6:n.1764+129_1764+130insGA
NM_022166.3:c.1764+129_1764+130insGA	NP_071449.1:n.1764+129_1764+130insGA
XM_011522574.1:c.1764+129_1764+130insGA	XP_011520876.1:n.1764+129_1764+130insGA
XR_933140.1:n.336-16_336-15insCT
XR_933141.1:n.175-16_175-15insCT
XR_933143.1:n.237-16_237-15insCT
NR_135179.1:n.147-16_147-15insCT
XM_017023539.2:c.1764+129_1764+130insGA	XP_016879028.1:n.1764+129_1764+130insGA
XM_017023540.2:c.1764+129_1764+130insGA	XP_016879029.1:n.1764+129_1764+130insGA
NM_022166.4:c.1764+129_1764+130insGA MANE Select	NP_071449.1:n.1764+129_1764+130insGA