Canonical Allele Identifier: CA2210541519
Gene: XYLT1 HGNC NCBI

Linked Data

dbSNP Id: rs2030823335

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17138182_17138183insTAGAACATCCTTGAAGT , CM000678.2:g.17138182_17138183insTAGAACATCCTTGAAGT GRCh38
NC_000016.9:g.17232039_17232040insTAGAACATCCTTGAAGT , CM000678.1:g.17232039_17232040insTAGAACATCCTTGAAGT GRCh37
NC_000016.8:g.17139540_17139541insTAGAACATCCTTGAAGT NCBI36
NG_015843.1:g.337705_337706insAGGATGTTCTAACTTCA
NG_015843.2:g.337705_337706insAGGATGTTCTAACTTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1764+178_1764+179insAGGATGTTCTAACTTCA MANE Select ENSP00000261381.6:n.1764+178_1764+179insAGGATGTTCTAACTTCA
ENST00000261381.6:c.1764+178_1764+179insAGGATGTTCTAACTTCA ENSP00000261381.6:n.1764+178_1764+179insAGGATGTTCTAACTTCA
NM_022166.3:c.1764+178_1764+179insAGGATGTTCTAACTTCA NP_071449.1:n.1764+178_1764+179insAGGATGTTCTAACTTCA
XM_011522574.1:c.1764+178_1764+179insAGGATGTTCTAACTTCA XP_011520876.1:n.1764+178_1764+179insAGGATGTTCTAACTTCA
XR_933140.1:n.336-60_336-59insTAGAACATCCTTGAAGT
XR_933141.1:n.175-60_175-59insTAGAACATCCTTGAAGT
XR_933143.1:n.237-60_237-59insTAGAACATCCTTGAAGT
NR_135179.1:n.147-60_147-59insTAGAACATCCTTGAAGT
XM_017023539.2:c.1764+178_1764+179insAGGATGTTCTAACTTCA XP_016879028.1:n.1764+178_1764+179insAGGATGTTCTAACTTCA
XM_017023540.2:c.1764+178_1764+179insAGGATGTTCTAACTTCA XP_016879029.1:n.1764+178_1764+179insAGGATGTTCTAACTTCA
NM_022166.4:c.1764+178_1764+179insAGGATGTTCTAACTTCA MANE Select NP_071449.1:n.1764+178_1764+179insAGGATGTTCTAACTTCA