Canonical Allele Identifier: CA2631987353

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138177-T-TGAAGTTAGAACATCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138182_17138183insTAGAACATCCCCGAAGT , CM000678.2:g.17138182_17138183insTAGAACATCCCCGAAGT	GRCh38
NC_000016.9:g.17232039_17232040insTAGAACATCCCCGAAGT , CM000678.1:g.17232039_17232040insTAGAACATCCCCGAAGT	GRCh37
NC_000016.8:g.17139540_17139541insTAGAACATCCCCGAAGT	NCBI36
NG_015843.1:g.337704_337705insGGGGATGTTCTAACTTC
NG_015843.2:g.337704_337705insGGGGATGTTCTAACTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+177_1764+178insGGGGATGTTCTAACTTC MANE Select	ENSP00000261381.6:n.1764+177_1764+178insGGGGATGTTCTAACTTC
ENST00000261381.6:c.1764+177_1764+178insGGGGATGTTCTAACTTC	ENSP00000261381.6:n.1764+177_1764+178insGGGGATGTTCTAACTTC
NM_022166.3:c.1764+177_1764+178insGGGGATGTTCTAACTTC	NP_071449.1:n.1764+177_1764+178insGGGGATGTTCTAACTTC
XM_011522574.1:c.1764+177_1764+178insGGGGATGTTCTAACTTC	XP_011520876.1:n.1764+177_1764+178insGGGGATGTTCTAACTTC
XR_933140.1:n.336-60_336-59insTAGAACATCCCCGAAGT
XR_933141.1:n.175-60_175-59insTAGAACATCCCCGAAGT
XR_933143.1:n.237-60_237-59insTAGAACATCCCCGAAGT
NR_135179.1:n.147-60_147-59insTAGAACATCCCCGAAGT
XM_017023539.2:c.1764+177_1764+178insGGGGATGTTCTAACTTC	XP_016879028.1:n.1764+177_1764+178insGGGGATGTTCTAACTTC
XM_017023540.2:c.1764+177_1764+178insGGGGATGTTCTAACTTC	XP_016879029.1:n.1764+177_1764+178insGGGGATGTTCTAACTTC
NM_022166.4:c.1764+177_1764+178insGGGGATGTTCTAACTTC MANE Select	NP_071449.1:n.1764+177_1764+178insGGGGATGTTCTAACTTC