Canonical Allele Identifier: CA2631987315

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138163-G-GAA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138163_17138164insAA , CM000678.2:g.17138163_17138164insAA	GRCh38
NC_000016.9:g.17232020_17232021insAA , CM000678.1:g.17232020_17232021insAA	GRCh37
NC_000016.8:g.17139521_17139522insAA	NCBI36
NG_015843.1:g.337718_337719insTT
NG_015843.2:g.337718_337719insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+191_1764+192insTT MANE Select	ENSP00000261381.6:n.1764+191_1764+192insTT
ENST00000261381.6:c.1764+191_1764+192insTT	ENSP00000261381.6:n.1764+191_1764+192insTT
NM_022166.3:c.1764+191_1764+192insTT	NP_071449.1:n.1764+191_1764+192insTT
XM_011522574.1:c.1764+191_1764+192insTT	XP_011520876.1:n.1764+191_1764+192insTT
XR_933140.1:n.336-79_336-78insAA
XR_933141.1:n.175-79_175-78insAA
XR_933143.1:n.237-79_237-78insAA
NR_135179.1:n.147-79_147-78insAA
XM_017023539.2:c.1764+191_1764+192insTT	XP_016879028.1:n.1764+191_1764+192insTT
XM_017023540.2:c.1764+191_1764+192insTT	XP_016879029.1:n.1764+191_1764+192insTT
NM_022166.4:c.1764+191_1764+192insTT MANE Select	NP_071449.1:n.1764+191_1764+192insTT