Canonical Allele Identifier: CA2631987359

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138179-A-AAGTTAGAACATCCCTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138182_17138183insTAGAACATCCCTGTAGT , CM000678.2:g.17138182_17138183insTAGAACATCCCTGTAGT	GRCh38
NC_000016.9:g.17232039_17232040insTAGAACATCCCTGTAGT , CM000678.1:g.17232039_17232040insTAGAACATCCCTGTAGT	GRCh37
NC_000016.8:g.17139540_17139541insTAGAACATCCCTGTAGT	NCBI36
NG_015843.1:g.337702_337703insACAGGGATGTTCTAACT
NG_015843.2:g.337702_337703insACAGGGATGTTCTAACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+175_1764+176insACAGGGATGTTCTAACT MANE Select	ENSP00000261381.6:n.1764+175_1764+176insACAGGGATGTTCTAACT
ENST00000261381.6:c.1764+175_1764+176insACAGGGATGTTCTAACT	ENSP00000261381.6:n.1764+175_1764+176insACAGGGATGTTCTAACT
NM_022166.3:c.1764+175_1764+176insACAGGGATGTTCTAACT	NP_071449.1:n.1764+175_1764+176insACAGGGATGTTCTAACT
XM_011522574.1:c.1764+175_1764+176insACAGGGATGTTCTAACT	XP_011520876.1:n.1764+175_1764+176insACAGGGATGTTCTAACT
XR_933140.1:n.336-60_336-59insTAGAACATCCCTGTAGT
XR_933141.1:n.175-60_175-59insTAGAACATCCCTGTAGT
XR_933143.1:n.237-60_237-59insTAGAACATCCCTGTAGT
NR_135179.1:n.147-60_147-59insTAGAACATCCCTGTAGT
XM_017023539.2:c.1764+175_1764+176insACAGGGATGTTCTAACT	XP_016879028.1:n.1764+175_1764+176insACAGGGATGTTCTAACT
XM_017023540.2:c.1764+175_1764+176insACAGGGATGTTCTAACT	XP_016879029.1:n.1764+175_1764+176insACAGGGATGTTCTAACT
NM_022166.4:c.1764+175_1764+176insACAGGGATGTTCTAACT MANE Select	NP_071449.1:n.1764+175_1764+176insACAGGGATGTTCTAACT