Canonical Allele Identifier: CA2631987577

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138583-T-TGAACTGGGGTGGGAAATGGTGAACC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138584_17138608dup , CM000678.2:g.17138584_17138608dup	GRCh38
NC_000016.9:g.17232441_17232465dup , CM000678.1:g.17232441_17232465dup	GRCh37
NC_000016.8:g.17139942_17139966dup	NCBI36
NG_015843.1:g.337274_337298dup
NG_015843.2:g.337274_337298dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-77_1588-53dup MANE Select	ENSP00000261381.6:n.1588-77_1588-53dup
ENST00000261381.6:c.1588-77_1588-53dup	ENSP00000261381.6:n.1588-77_1588-53dup
NM_022166.3:c.1588-77_1588-53dup	NP_071449.1:n.1588-77_1588-53dup
XM_011522574.1:c.1588-77_1588-53dup	XP_011520876.1:n.1588-77_1588-53dup
XR_933141.1:n.517_541dup
NR_135179.1:n.489_513dup
XM_017023539.2:c.1588-77_1588-53dup	XP_016879028.1:n.1588-77_1588-53dup
XM_017023540.2:c.1588-77_1588-53dup	XP_016879029.1:n.1588-77_1588-53dup
NM_022166.4:c.1588-77_1588-53dup MANE Select	NP_071449.1:n.1588-77_1588-53dup