Canonical Allele Identifier: CA621654977

Gene: XYLT1

Linked Data

• dbSNP Id: rs143943003
• gnomAD v2: 16-17232020-G-GGTTAGAACATCCCTGAAGTTAGAACATCCCTGAA
• gnomAD v3: 16-17138163-G-GGTTAGAACATCCCTGAAGTTAGAACATCCCTGAA
• gnomAD v4: 16-17138163-G-GGTTAGAACATCCCTGAAGTTAGAACATCCCTGAA
• MyVariant Identifiers: chr16:g.17232020_17232021insGTTAGAACATCCCTGAAGTTAGAACATCCCTGAA (hg19) ; chr16:g.17138163_17138164insGTTAGAACATCCCTGAAGTTAGAACATCCCTGAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138182_17138183insTAGAACATCCCTGAAGTTAGAACATCCCTGAAGT , CM000678.2:g.17138182_17138183insTAGAACATCCCTGAAGTTAGAACATCCCTGAAGT	GRCh38
NC_000016.9:g.17232039_17232040insTAGAACATCCCTGAAGTTAGAACATCCCTGAAGT , CM000678.1:g.17232039_17232040insTAGAACATCCCTGAAGTTAGAACATCCCTGAAGT	GRCh37
NC_000016.8:g.17139540_17139541insTAGAACATCCCTGAAGTTAGAACATCCCTGAAGT	NCBI36
NG_015843.1:g.337718_337719insTTCAGGGATGTTCTAACTTCAGGGATGTTCTAAC
NG_015843.2:g.337718_337719insTTCAGGGATGTTCTAACTTCAGGGATGTTCTAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+191_1764+192insTTCAGGGATGTTCTAACTTCAGGGATGTTCTAAC MANE Select	ENSP00000261381.6:n.1764+191_1764+192insTTCAGGGATGTTCTAACTTCA...
ENST00000261381.6:c.1764+191_1764+192insTTCAGGGATGTTCTAACTTCAGGGATGTTCTAAC	ENSP00000261381.6:n.1764+191_1764+192insTTCAGGGATGTTCTAACTTCA...
NM_022166.3:c.1764+191_1764+192insTTCAGGGATGTTCTAACTTCAGGGATGTTCTAAC	NP_071449.1:n.1764+191_1764+192insTTCAGGGATGTTCTAACTTCAGGGATG...
XM_011522574.1:c.1764+191_1764+192insTTCAGGGATGTTCTAACTTCAGGGATGTTCTAAC	XP_011520876.1:n.1764+191_1764+192insTTCAGGGATGTTCTAACTTCAGGG...
XR_933140.1:n.336-60_336-59insTAGAACATCCCTGAAGTTAGAACATCCCTGAAGT
XR_933141.1:n.175-60_175-59insTAGAACATCCCTGAAGTTAGAACATCCCTGAAGT
XR_933143.1:n.237-60_237-59insTAGAACATCCCTGAAGTTAGAACATCCCTGAAGT
NR_135179.1:n.147-60_147-59insTAGAACATCCCTGAAGTTAGAACATCCCTGAAGT
XM_017023539.2:c.1764+191_1764+192insTTCAGGGATGTTCTAACTTCAGGGATGTTCTAAC	XP_016879028.1:n.1764+191_1764+192insTTCAGGGATGTTCTAACTTCAGGG...
XM_017023540.2:c.1764+191_1764+192insTTCAGGGATGTTCTAACTTCAGGGATGTTCTAAC	XP_016879029.1:n.1764+191_1764+192insTTCAGGGATGTTCTAACTTCAGGG...
NM_022166.4:c.1764+191_1764+192insTTCAGGGATGTTCTAACTTCAGGGATGTTCTAAC MANE Select	NP_071449.1:n.1764+191_1764+192insTTCAGGGATGTTCTAACTTCAGGGATG...