Canonical Allele Identifier: CA621656022

Gene: XYLT1

Linked Data

• dbSNP Id: rs1567291306
• gnomAD v2: 16-17232202-A-AAAGT
• gnomAD v4: 16-17138345-A-AAAGT
• MyVariant Identifiers: chr16:g.17232202_17232203insAAGT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138346_17138349dup , CM000678.2:g.17138346_17138349dup	GRCh38
NC_000016.9:g.17232203_17232206dup , CM000678.1:g.17232203_17232206dup	GRCh37
NC_000016.8:g.17139704_17139707dup	NCBI36
NG_015843.1:g.337533_337536dup
NG_015843.2:g.337533_337536dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+6_1764+9dup MANE Select	ENSP00000261381.6:n.1764+6_1764+9dup
ENST00000261381.6:c.1764+6_1764+9dup	ENSP00000261381.6:n.1764+6_1764+9dup
NM_022166.3:c.1764+6_1764+9dup	NP_071449.1:n.1764+6_1764+9dup
XM_011522574.1:c.1764+6_1764+9dup	XP_011520876.1:n.1764+6_1764+9dup
XR_933141.1:n.279_282dup
NR_135179.1:n.251_254dup
XM_017023539.2:c.1764+6_1764+9dup	XP_016879028.1:n.1764+6_1764+9dup
XM_017023540.2:c.1764+6_1764+9dup	XP_016879029.1:n.1764+6_1764+9dup
NM_022166.4:c.1764+6_1764+9dup MANE Select	NP_071449.1:n.1764+6_1764+9dup