Canonical Allele Identifier: CA2631987468
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138224_17138227del , CM000678.2:g.17138224_17138227del GRCh38
NC_000016.9:g.17232081_17232084del , CM000678.1:g.17232081_17232084del GRCh37
NC_000016.8:g.17139582_17139585del NCBI36
NG_015843.1:g.337655_337658del
NG_015843.2:g.337655_337658del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1764+128_1764+131del MANE Select ENSP00000261381.6:n.1764+128_1764+131del
ENST00000261381.6:c.1764+128_1764+131del ENSP00000261381.6:n.1764+128_1764+131del
NM_022166.3:c.1764+128_1764+131del NP_071449.1:n.1764+128_1764+131del
XM_011522574.1:c.1764+128_1764+131del XP_011520876.1:n.1764+128_1764+131del
XR_933140.1:n.336-18_336-15del
XR_933141.1:n.175-18_175-15del
XR_933143.1:n.237-18_237-15del
NR_135179.1:n.147-18_147-15del
XM_017023539.2:c.1764+128_1764+131del XP_016879028.1:n.1764+128_1764+131del
XM_017023540.2:c.1764+128_1764+131del XP_016879029.1:n.1764+128_1764+131del
NM_022166.4:c.1764+128_1764+131del MANE Select NP_071449.1:n.1764+128_1764+131del