Canonical Allele Identifier: CA2631987458

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138220-A-AAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138221_17138222insTA , CM000678.2:g.17138221_17138222insTA	GRCh38
NC_000016.9:g.17232078_17232079insTA , CM000678.1:g.17232078_17232079insTA	GRCh37
NC_000016.8:g.17139579_17139580insTA	NCBI36
NG_015843.1:g.337661_337662insAT
NG_015843.2:g.337661_337662insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+134_1764+135insAT MANE Select	ENSP00000261381.6:n.1764+134_1764+135insAT
ENST00000261381.6:c.1764+134_1764+135insAT	ENSP00000261381.6:n.1764+134_1764+135insAT
NM_022166.3:c.1764+134_1764+135insAT	NP_071449.1:n.1764+134_1764+135insAT
XM_011522574.1:c.1764+134_1764+135insAT	XP_011520876.1:n.1764+134_1764+135insAT
XR_933140.1:n.336-21_336-20insTA
XR_933141.1:n.175-21_175-20insTA
XR_933143.1:n.237-21_237-20insTA
NR_135179.1:n.147-21_147-20insTA
XM_017023539.2:c.1764+134_1764+135insAT	XP_016879028.1:n.1764+134_1764+135insAT
XM_017023540.2:c.1764+134_1764+135insAT	XP_016879029.1:n.1764+134_1764+135insAT
NM_022166.4:c.1764+134_1764+135insAT MANE Select	NP_071449.1:n.1764+134_1764+135insAT