Canonical Allele Identifier: CA2631987549
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138346_17138380dup , CM000678.2:g.17138346_17138380dup GRCh38
NC_000016.9:g.17232203_17232237dup , CM000678.1:g.17232203_17232237dup GRCh37
NC_000016.8:g.17139704_17139738dup NCBI36
NG_015843.1:g.337502_337536dup
NG_015843.2:g.337502_337536dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1739_1764+9dup
ENST00000261381.6:c.1739_1764+9dup
NM_022166.3:c.1739_1764+9dup
XM_011522574.1:c.1739_1764+9dup
XR_933141.1:n.279_313dup
NR_135179.1:n.251_285dup
XM_017023539.2:c.1739_1764+9dup
XM_017023540.2:c.1739_1764+9dup
NM_022166.4:c.1739_1764+9dup