Canonical Allele Identifier: CA395219456
Gene: XYLT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.17134548A>G , CM000678.2:g.17134548A>G GRCh38
NC_000016.9:g.17228405A>G , CM000678.1:g.17228405A>G GRCh37
NC_000016.8:g.17135906A>G NCBI36
NG_015843.1:g.341334T>C
NG_015843.2:g.341334T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261381.7:c.1952T>C MANE Select ENSP00000261381.6:p.Leu651Ser
ENST00000261381.6:c.1952T>C ENSP00000261381.6:p.Leu651Ser
NM_022166.3:c.1952T>C NP_071449.1:p.Leu651Ser
XM_011522574.1:c.1952T>C XP_011520876.1:p.Leu651Ser
XR_933140.1:n.80A>G
XR_933141.1:n.73A>G
XR_933143.1:n.80A>G
NR_135179.1:n.45A>G
XM_017023539.2:c.1952T>C XP_016879028.1:p.Leu651Ser
XM_017023540.2:c.1952T>C XP_016879029.1:p.Leu651Ser
NM_022166.4:c.1952T>C MANE Select NP_071449.1:p.Leu651Ser