Canonical Allele Identifier: CA2631987324

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138163-G-GGTTAGAAAATCCCTGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138170_17138171insAATCCCTGAAGTTAGAA , CM000678.2:g.17138170_17138171insAATCCCTGAAGTTAGAA	GRCh38
NC_000016.9:g.17232027_17232028insAATCCCTGAAGTTAGAA , CM000678.1:g.17232027_17232028insAATCCCTGAAGTTAGAA	GRCh37
NC_000016.8:g.17139528_17139529insAATCCCTGAAGTTAGAA	NCBI36
NG_015843.1:g.337718_337719insTTCAGGGATTTTCTAAC
NG_015843.2:g.337718_337719insTTCAGGGATTTTCTAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+191_1764+192insTTCAGGGATTTTCTAAC MANE Select	ENSP00000261381.6:n.1764+191_1764+192insTTCAGGGATTTTCTAAC
ENST00000261381.6:c.1764+191_1764+192insTTCAGGGATTTTCTAAC	ENSP00000261381.6:n.1764+191_1764+192insTTCAGGGATTTTCTAAC
NM_022166.3:c.1764+191_1764+192insTTCAGGGATTTTCTAAC	NP_071449.1:n.1764+191_1764+192insTTCAGGGATTTTCTAAC
XM_011522574.1:c.1764+191_1764+192insTTCAGGGATTTTCTAAC	XP_011520876.1:n.1764+191_1764+192insTTCAGGGATTTTCTAAC
XR_933140.1:n.336-72_336-71insAATCCCTGAAGTTAGAA
XR_933141.1:n.175-72_175-71insAATCCCTGAAGTTAGAA
XR_933143.1:n.237-72_237-71insAATCCCTGAAGTTAGAA
NR_135179.1:n.147-72_147-71insAATCCCTGAAGTTAGAA
XM_017023539.2:c.1764+191_1764+192insTTCAGGGATTTTCTAAC	XP_016879028.1:n.1764+191_1764+192insTTCAGGGATTTTCTAAC
XM_017023540.2:c.1764+191_1764+192insTTCAGGGATTTTCTAAC	XP_016879029.1:n.1764+191_1764+192insTTCAGGGATTTTCTAAC
NM_022166.4:c.1764+191_1764+192insTTCAGGGATTTTCTAAC MANE Select	NP_071449.1:n.1764+191_1764+192insTTCAGGGATTTTCTAAC