Canonical Allele Identifier: CA2210541580

Gene: XYLT1

Linked Data

• dbSNP Id: rs2030827143
• gnomAD v4: 16-17138222-C-CTATT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138223_17138226dup , CM000678.2:g.17138223_17138226dup	GRCh38
NC_000016.9:g.17232080_17232083dup , CM000678.1:g.17232080_17232083dup	GRCh37
NC_000016.8:g.17139581_17139584dup	NCBI36
NG_015843.1:g.337656_337659dup
NG_015843.2:g.337656_337659dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+129_1764+132dup MANE Select	ENSP00000261381.6:n.1764+129_1764+132dup
ENST00000261381.6:c.1764+129_1764+132dup	ENSP00000261381.6:n.1764+129_1764+132dup
NM_022166.3:c.1764+129_1764+132dup	NP_071449.1:n.1764+129_1764+132dup
XM_011522574.1:c.1764+129_1764+132dup	XP_011520876.1:n.1764+129_1764+132dup
XR_933140.1:n.336-19_336-16dup
XR_933141.1:n.175-19_175-16dup
XR_933143.1:n.237-19_237-16dup
NR_135179.1:n.147-19_147-16dup
XM_017023539.2:c.1764+129_1764+132dup	XP_016879028.1:n.1764+129_1764+132dup
XM_017023540.2:c.1764+129_1764+132dup	XP_016879029.1:n.1764+129_1764+132dup
NM_022166.4:c.1764+129_1764+132dup MANE Select	NP_071449.1:n.1764+129_1764+132dup