Canonical Allele Identifier: CA2631987640

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138751-T-TTCATAGCAATGCAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138753_17138769dup , CM000678.2:g.17138753_17138769dup	GRCh38
NC_000016.9:g.17232610_17232626dup , CM000678.1:g.17232610_17232626dup	GRCh37
NC_000016.8:g.17140111_17140127dup	NCBI36
NG_015843.1:g.337114_337130dup
NG_015843.2:g.337114_337130dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-237_1588-221dup MANE Select	ENSP00000261381.6:n.1588-237_1588-221dup
ENST00000261381.6:c.1588-237_1588-221dup	ENSP00000261381.6:n.1588-237_1588-221dup
NM_022166.3:c.1588-237_1588-221dup	NP_071449.1:n.1588-237_1588-221dup
XM_011522574.1:c.1588-237_1588-221dup	XP_011520876.1:n.1588-237_1588-221dup
XM_017023539.2:c.1588-237_1588-221dup	XP_016879028.1:n.1588-237_1588-221dup
XM_017023540.2:c.1588-237_1588-221dup	XP_016879029.1:n.1588-237_1588-221dup
NM_022166.4:c.1588-237_1588-221dup MANE Select	NP_071449.1:n.1588-237_1588-221dup