Canonical Allele Identifier: CA718616271

Gene: XYLT1

Linked Data

• dbSNP Id: rs1461800162
• gnomAD v3: 16-17138172-A-ATCCCTGAAGT
• gnomAD v4: 16-17138172-A-ATCCCTGAAGT
• MyVariant Identifiers: chr16:g.17232029_17232030insTCCCTGAAGT (hg19) ; chr16:g.17138172_17138173insTCCCTGAAGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138173_17138182dup , CM000678.2:g.17138173_17138182dup	GRCh38
NC_000016.9:g.17232030_17232039dup , CM000678.1:g.17232030_17232039dup	GRCh37
NC_000016.8:g.17139531_17139540dup	NCBI36
NG_015843.1:g.337700_337709dup
NG_015843.2:g.337700_337709dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+173_1764+182dup MANE Select	ENSP00000261381.6:n.1764+173_1764+182dup
ENST00000261381.6:c.1764+173_1764+182dup	ENSP00000261381.6:n.1764+173_1764+182dup
NM_022166.3:c.1764+173_1764+182dup	NP_071449.1:n.1764+173_1764+182dup
XM_011522574.1:c.1764+173_1764+182dup	XP_011520876.1:n.1764+173_1764+182dup
XR_933140.1:n.336-69_336-60dup
XR_933141.1:n.175-69_175-60dup
XR_933143.1:n.237-69_237-60dup
NR_135179.1:n.147-69_147-60dup
XM_017023539.2:c.1764+173_1764+182dup	XP_016879028.1:n.1764+173_1764+182dup
XM_017023540.2:c.1764+173_1764+182dup	XP_016879029.1:n.1764+173_1764+182dup
NM_022166.4:c.1764+173_1764+182dup MANE Select	NP_071449.1:n.1764+173_1764+182dup