Canonical Allele Identifier: CA7927858

Gene: XYLT1

Linked Data

• dbSNP Id: rs766749500
• ExAC: 16:17232416 A / AGCAGGGGAGAGAGG
• MyVariant Identifiers: chr16:g.17232416_17232417insGCAGGGGAGAGAGG (hg19) ; chr16:g.17138559_17138560insGCAGGGGAGAGAGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138560_17138561insCAGGGGAGAGAGGG , CM000678.2:g.17138560_17138561insCAGGGGAGAGAGGG	GRCh38
NC_000016.9:g.17232417_17232418insCAGGGGAGAGAGGG , CM000678.1:g.17232417_17232418insCAGGGGAGAGAGGG	GRCh37
NC_000016.8:g.17139918_17139919insCAGGGGAGAGAGGG	NCBI36
NG_015843.1:g.337322_337323insCCTCTCTCCCCTGC
NG_015843.2:g.337322_337323insCCTCTCTCCCCTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-29_1588-28insCCTCTCTCCCCTGC MANE Select	ENSP00000261381.6:n.1588-29_1588-28insCCTCTCTCCCCTGC
ENST00000261381.6:c.1588-29_1588-28insCCTCTCTCCCCTGC	ENSP00000261381.6:n.1588-29_1588-28insCCTCTCTCCCCTGC
NM_022166.3:c.1588-29_1588-28insCCTCTCTCCCCTGC	NP_071449.1:n.1588-29_1588-28insCCTCTCTCCCCTGC
XM_011522574.1:c.1588-29_1588-28insCCTCTCTCCCCTGC	XP_011520876.1:n.1588-29_1588-28insCCTCTCTCCCCTGC
XR_933141.1:n.493_494insCAGGGGAGAGAGGG
NR_135179.1:n.465_466insCAGGGGAGAGAGGG
XM_017023539.2:c.1588-29_1588-28insCCTCTCTCCCCTGC	XP_016879028.1:n.1588-29_1588-28insCCTCTCTCCCCTGC
XM_017023540.2:c.1588-29_1588-28insCCTCTCTCCCCTGC	XP_016879029.1:n.1588-29_1588-28insCCTCTCTCCCCTGC
NM_022166.4:c.1588-29_1588-28insCCTCTCTCCCCTGC MANE Select	NP_071449.1:n.1588-29_1588-28insCCTCTCTCCCCTGC