Canonical Allele Identifier: CA975206154

Gene: XYLT1

Linked Data

• dbSNP Id: rs2030876520
• gnomAD v3: 16-17138992-C-CAGACGGCAACATAGGGA
• gnomAD v4: 16-17138992-C-CAGACGGCAACATAGGGA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138995_17139011dup , CM000678.2:g.17138995_17139011dup	GRCh38
NC_000016.9:g.17232852_17232868dup , CM000678.1:g.17232852_17232868dup	GRCh37
NC_000016.8:g.17140353_17140369dup	NCBI36
NG_015843.1:g.336873_336889dup
NG_015843.2:g.336873_336889dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-478_1588-462dup MANE Select	ENSP00000261381.6:n.1588-478_1588-462dup
ENST00000261381.6:c.1588-478_1588-462dup	ENSP00000261381.6:n.1588-478_1588-462dup
NM_022166.3:c.1588-478_1588-462dup	NP_071449.1:n.1588-478_1588-462dup
XM_011522574.1:c.1588-478_1588-462dup	XP_011520876.1:n.1588-478_1588-462dup
XM_017023539.2:c.1588-478_1588-462dup	XP_016879028.1:n.1588-478_1588-462dup
XM_017023540.2:c.1588-478_1588-462dup	XP_016879029.1:n.1588-478_1588-462dup
NM_022166.4:c.1588-478_1588-462dup MANE Select	NP_071449.1:n.1588-478_1588-462dup