Canonical Allele Identifier: CA2631987603

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138682-G-GTACAGCTTGGAGAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138691_17138692insGAGAACTACAGCTTG , CM000678.2:g.17138691_17138692insGAGAACTACAGCTTG	GRCh38
NC_000016.9:g.17232548_17232549insGAGAACTACAGCTTG , CM000678.1:g.17232548_17232549insGAGAACTACAGCTTG	GRCh37
NC_000016.8:g.17140049_17140050insGAGAACTACAGCTTG	NCBI36
NG_015843.1:g.337199_337200insGTTCTCCAAGCTGTA
NG_015843.2:g.337199_337200insGTTCTCCAAGCTGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-152_1588-151insGTTCTCCAAGCTGTA MANE Select	ENSP00000261381.6:n.1588-152_1588-151insGTTCTCCAAGCTGTA
ENST00000261381.6:c.1588-152_1588-151insGTTCTCCAAGCTGTA	ENSP00000261381.6:n.1588-152_1588-151insGTTCTCCAAGCTGTA
NM_022166.3:c.1588-152_1588-151insGTTCTCCAAGCTGTA	NP_071449.1:n.1588-152_1588-151insGTTCTCCAAGCTGTA
XM_011522574.1:c.1588-152_1588-151insGTTCTCCAAGCTGTA	XP_011520876.1:n.1588-152_1588-151insGTTCTCCAAGCTGTA
XR_933141.1:n.624_625insGAGAACTACAGCTTG
NR_135179.1:n.596_597insGAGAACTACAGCTTG
XM_017023539.2:c.1588-152_1588-151insGTTCTCCAAGCTGTA	XP_016879028.1:n.1588-152_1588-151insGTTCTCCAAGCTGTA
XM_017023540.2:c.1588-152_1588-151insGTTCTCCAAGCTGTA	XP_016879029.1:n.1588-152_1588-151insGTTCTCCAAGCTGTA
NM_022166.4:c.1588-152_1588-151insGTTCTCCAAGCTGTA MANE Select	NP_071449.1:n.1588-152_1588-151insGTTCTCCAAGCTGTA