Canonical Allele Identifier: CA2581914044

Gene: XXYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.195137645G>T , CM000665.2:g.195137645G>T	GRCh38
NC_000003.11:g.194858374G>T , CM000665.1:g.194858374G>T	GRCh37
NC_000003.10:g.196339663G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_152531.5:c.785+18804C>A MANE Select	NP_689744.3:n.785+18804C>A
ENST00000310380.11:c.785+18804C>A MANE Select	ENSP00000309640.6:n.785+18804C>A
NM_001308069.1:c.347+18804C>A	NP_001294998.1:n.347+18804C>A
NM_001308069.2:c.347+18804C>A	NP_001294998.1:n.347+18804C>A
NM_152531.4:c.785+18804C>A	NP_689744.3:n.785+18804C>A
ENST00000310380.10:c.785+18804C>A	ENSP00000309640.6:n.785+18804C>A
ENST00000418940.5:c.*166+18804C>A	ENSP00000393989.1:n.*166+18804C>A
ENST00000429994.5:c.347+18804C>A	ENSP00000399422.1:n.347+18804C>A
ENST00000437101.5:c.176+18804C>A	ENSP00000409865.1:n.176+18804C>A
ENST00000473200.1:n.217+16242C>A
ENST00000491138.1:n.663+18804C>A
XM_005269285.2:c.224+18804C>A	XP_005269342.1:n.224+18804C>A
XM_005269286.3:c.224+18804C>A	XP_005269343.1:n.224+18804C>A
XM_005269286.5:c.224+18804C>A	XP_005269343.1:n.224+18804C>A
XM_005269288.2:c.224+18804C>A	XP_005269345.1:n.224+18804C>A
XM_006713511.2:c.224+18804C>A	XP_006713574.1:n.224+18804C>A
XM_006713512.2:c.188+18804C>A	XP_006713575.1:n.188+18804C>A
XM_011512448.1:c.224+18804C>A	XP_011510750.1:n.224+18804C>A
XM_011512448.3:c.224+18804C>A	XP_011510750.1:n.224+18804C>A
XM_011512449.1:c.188+18804C>A	XP_011510751.1:n.188+18804C>A
XM_011512450.1:c.188+18804C>A	XP_011510752.1:n.188+18804C>A
XM_017005750.2:c.176+18804C>A	XP_016861239.1:n.176+18804C>A
XR_924104.1:n.864+18804C>A