Canonical Allele Identifier: CA2631987550

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138348-G-GTCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138349_17138352dup , CM000678.2:g.17138349_17138352dup	GRCh38
NC_000016.9:g.17232206_17232209dup , CM000678.1:g.17232206_17232209dup	GRCh37
NC_000016.8:g.17139707_17139710dup	NCBI36
NG_015843.1:g.337530_337533dup
NG_015843.2:g.337530_337533dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+3_1764+6dup MANE Select	ENSP00000261381.6:n.1764+3_1764+6dup
ENST00000261381.6:c.1764+3_1764+6dup	ENSP00000261381.6:n.1764+3_1764+6dup
NM_022166.3:c.1764+3_1764+6dup	NP_071449.1:n.1764+3_1764+6dup
XM_011522574.1:c.1764+3_1764+6dup	XP_011520876.1:n.1764+3_1764+6dup
XR_933141.1:n.282_285dup
NR_135179.1:n.254_257dup
XM_017023539.2:c.1764+3_1764+6dup	XP_016879028.1:n.1764+3_1764+6dup
XM_017023540.2:c.1764+3_1764+6dup	XP_016879029.1:n.1764+3_1764+6dup
NM_022166.4:c.1764+3_1764+6dup MANE Select	NP_071449.1:n.1764+3_1764+6dup