Canonical Allele Identifier: CA2631987189

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138113-G-GGAATAATAATGAAAGGTCATTTGTTGTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138114_17138142dup , CM000678.2:g.17138114_17138142dup	GRCh38
NC_000016.9:g.17231971_17231999dup , CM000678.1:g.17231971_17231999dup	GRCh37
NC_000016.8:g.17139472_17139500dup	NCBI36
NG_015843.1:g.337740_337768dup
NG_015843.2:g.337740_337768dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+213_1764+241dup MANE Select	ENSP00000261381.6:n.1764+213_1764+241dup
ENST00000261381.6:c.1764+213_1764+241dup	ENSP00000261381.6:n.1764+213_1764+241dup
NM_022166.3:c.1764+213_1764+241dup	NP_071449.1:n.1764+213_1764+241dup
XM_011522574.1:c.1764+213_1764+241dup	XP_011520876.1:n.1764+213_1764+241dup
XR_933140.1:n.336-128_336-100dup
XR_933141.1:n.175-128_175-100dup
XR_933143.1:n.237-128_237-100dup
NR_135179.1:n.147-128_147-100dup
XM_017023539.2:c.1764+213_1764+241dup	XP_016879028.1:n.1764+213_1764+241dup
XM_017023540.2:c.1764+213_1764+241dup	XP_016879029.1:n.1764+213_1764+241dup
NM_022166.4:c.1764+213_1764+241dup MANE Select	NP_071449.1:n.1764+213_1764+241dup