Canonical Allele Identifier: CA2631987514

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138263-T-TACC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138264_17138265insCCA , CM000678.2:g.17138264_17138265insCCA	GRCh38
NC_000016.9:g.17232121_17232122insCCA , CM000678.1:g.17232121_17232122insCCA	GRCh37
NC_000016.8:g.17139622_17139623insCCA	NCBI36
NG_015843.1:g.337618_337619insGGT
NG_015843.2:g.337618_337619insGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+91_1764+92insGGT MANE Select	ENSP00000261381.6:n.1764+91_1764+92insGGT
ENST00000261381.6:c.1764+91_1764+92insGGT	ENSP00000261381.6:n.1764+91_1764+92insGGT
NM_022166.3:c.1764+91_1764+92insGGT	NP_071449.1:n.1764+91_1764+92insGGT
XM_011522574.1:c.1764+91_1764+92insGGT	XP_011520876.1:n.1764+91_1764+92insGGT
XR_933140.1:n.358_359insCCA
XR_933141.1:n.197_198insCCA
XR_933143.1:n.259_260insCCA
NR_135179.1:n.169_170insCCA
XM_017023539.2:c.1764+91_1764+92insGGT	XP_016879028.1:n.1764+91_1764+92insGGT
XM_017023540.2:c.1764+91_1764+92insGGT	XP_016879029.1:n.1764+91_1764+92insGGT
NM_022166.4:c.1764+91_1764+92insGGT MANE Select	NP_071449.1:n.1764+91_1764+92insGGT