Canonical Allele Identifier: CA2631987191

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138114-G-GAATAATAATGAAAGGTCATT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138115_17138134dup , CM000678.2:g.17138115_17138134dup	GRCh38
NC_000016.9:g.17231972_17231991dup , CM000678.1:g.17231972_17231991dup	GRCh37
NC_000016.8:g.17139473_17139492dup	NCBI36
NG_015843.1:g.337748_337767dup
NG_015843.2:g.337748_337767dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+221_1764+240dup MANE Select	ENSP00000261381.6:n.1764+221_1764+240dup
ENST00000261381.6:c.1764+221_1764+240dup	ENSP00000261381.6:n.1764+221_1764+240dup
NM_022166.3:c.1764+221_1764+240dup	NP_071449.1:n.1764+221_1764+240dup
XM_011522574.1:c.1764+221_1764+240dup	XP_011520876.1:n.1764+221_1764+240dup
XR_933140.1:n.336-127_336-108dup
XR_933141.1:n.175-127_175-108dup
XR_933143.1:n.237-127_237-108dup
NR_135179.1:n.147-127_147-108dup
XM_017023539.2:c.1764+221_1764+240dup	XP_016879028.1:n.1764+221_1764+240dup
XM_017023540.2:c.1764+221_1764+240dup	XP_016879029.1:n.1764+221_1764+240dup
NM_022166.4:c.1764+221_1764+240dup MANE Select	NP_071449.1:n.1764+221_1764+240dup