Canonical Allele Identifier: CA7927849

Gene: XYLT1

Linked Data

• dbSNP Id: rs761970455
• ExAC: 16:17232402 A / AGG
• gnomAD v2: 16-17232402-A-AGG
• gnomAD v4: 16-17138545-A-AGG
• MyVariant Identifiers: chr16:g.17232402_17232403insGG (hg19) ; chr16:g.17138545_17138546insGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138547_17138548dup , CM000678.2:g.17138547_17138548dup	GRCh38
NC_000016.9:g.17232404_17232405dup , CM000678.1:g.17232404_17232405dup	GRCh37
NC_000016.8:g.17139905_17139906dup	NCBI36
NG_015843.1:g.337335_337336dup
NG_015843.2:g.337335_337336dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-16_1588-15dup MANE Select	ENSP00000261381.6:n.1588-16_1588-15dup
ENST00000261381.6:c.1588-16_1588-15dup	ENSP00000261381.6:n.1588-16_1588-15dup
NM_022166.3:c.1588-16_1588-15dup	NP_071449.1:n.1588-16_1588-15dup
XM_011522574.1:c.1588-16_1588-15dup	XP_011520876.1:n.1588-16_1588-15dup
XR_933141.1:n.480_481dup
NR_135179.1:n.452_453dup
XM_017023539.2:c.1588-16_1588-15dup	XP_016879028.1:n.1588-16_1588-15dup
XM_017023540.2:c.1588-16_1588-15dup	XP_016879029.1:n.1588-16_1588-15dup
NM_022166.4:c.1588-16_1588-15dup MANE Select	NP_071449.1:n.1588-16_1588-15dup