Canonical Allele Identifier: CA2631987291

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138162-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138162_17138163insC , CM000678.2:g.17138162_17138163insC	GRCh38
NC_000016.9:g.17232019_17232020insC , CM000678.1:g.17232019_17232020insC	GRCh37
NC_000016.8:g.17139520_17139521insC	NCBI36
NG_015843.1:g.337719_337720insG
NG_015843.2:g.337719_337720insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+192_1764+193insG MANE Select	ENSP00000261381.6:n.1764+192_1764+193insG
ENST00000261381.6:c.1764+192_1764+193insG	ENSP00000261381.6:n.1764+192_1764+193insG
NM_022166.3:c.1764+192_1764+193insG	NP_071449.1:n.1764+192_1764+193insG
XM_011522574.1:c.1764+192_1764+193insG	XP_011520876.1:n.1764+192_1764+193insG
XR_933140.1:n.336-80_336-79insC
XR_933141.1:n.175-80_175-79insC
XR_933143.1:n.237-80_237-79insC
NR_135179.1:n.147-80_147-79insC
XM_017023539.2:c.1764+192_1764+193insG	XP_016879028.1:n.1764+192_1764+193insG
XM_017023540.2:c.1764+192_1764+193insG	XP_016879029.1:n.1764+192_1764+193insG
NM_022166.4:c.1764+192_1764+193insG MANE Select	NP_071449.1:n.1764+192_1764+193insG