Canonical Allele Identifier: CA2631987333

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138165-T-TTAGAACATCCCTGAAGTAAGTGCTCAATAAACACTGGCTA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138167_17138206dup , CM000678.2:g.17138167_17138206dup	GRCh38
NC_000016.9:g.17232024_17232063dup , CM000678.1:g.17232024_17232063dup	GRCh37
NC_000016.8:g.17139525_17139564dup	NCBI36
NG_015843.1:g.337677_337716dup
NG_015843.2:g.337677_337716dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+150_1764+189dup MANE Select	ENSP00000261381.6:n.1764+150_1764+189dup
ENST00000261381.6:c.1764+150_1764+189dup	ENSP00000261381.6:n.1764+150_1764+189dup
NM_022166.3:c.1764+150_1764+189dup	NP_071449.1:n.1764+150_1764+189dup
XM_011522574.1:c.1764+150_1764+189dup	XP_011520876.1:n.1764+150_1764+189dup
XR_933140.1:n.336-75_336-36dup
XR_933141.1:n.175-75_175-36dup
XR_933143.1:n.237-75_237-36dup
NR_135179.1:n.147-75_147-36dup
XM_017023539.2:c.1764+150_1764+189dup	XP_016879028.1:n.1764+150_1764+189dup
XM_017023540.2:c.1764+150_1764+189dup	XP_016879029.1:n.1764+150_1764+189dup
NM_022166.4:c.1764+150_1764+189dup MANE Select	NP_071449.1:n.1764+150_1764+189dup