Canonical Allele Identifier: CA621656097

Gene: XYLT1

Linked Data

• dbSNP Id: rs1238529227
• gnomAD v2: 16-17232582-A-ATAAAT
• gnomAD v3: 16-17138725-A-ATAAAT
• gnomAD v4: 16-17138725-A-ATAAAT
• MyVariant Identifiers: chr16:g.17232582_17232583insTAAAT (hg19) ; chr16:g.17138725_17138726insTAAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138728_17138732dup , CM000678.2:g.17138728_17138732dup	GRCh38
NC_000016.9:g.17232585_17232589dup , CM000678.1:g.17232585_17232589dup	GRCh37
NC_000016.8:g.17140086_17140090dup	NCBI36
NG_015843.1:g.337152_337156dup
NG_015843.2:g.337152_337156dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-199_1588-195dup MANE Select	ENSP00000261381.6:n.1588-199_1588-195dup
ENST00000261381.6:c.1588-199_1588-195dup	ENSP00000261381.6:n.1588-199_1588-195dup
NM_022166.3:c.1588-199_1588-195dup	NP_071449.1:n.1588-199_1588-195dup
XM_011522574.1:c.1588-199_1588-195dup	XP_011520876.1:n.1588-199_1588-195dup
XM_017023539.2:c.1588-199_1588-195dup	XP_016879028.1:n.1588-199_1588-195dup
XM_017023540.2:c.1588-199_1588-195dup	XP_016879029.1:n.1588-199_1588-195dup
NM_022166.4:c.1588-199_1588-195dup MANE Select	NP_071449.1:n.1588-199_1588-195dup