Canonical Allele Identifier: CA2830536202

Gene: XXYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.195226495del , CM000665.2:g.195226495del	GRCh38
NC_000003.11:g.194947224del , CM000665.1:g.194947224del	GRCh37
NC_000003.10:g.196428513del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310380.11:c.652+216del MANE Select	ENSP00000309640.6:n.652+216del
ENST00000310380.10:c.652+216del	ENSP00000309640.6:n.652+216del
ENST00000418940.5:c.214+216del	ENSP00000393989.1:n.214+216del
ENST00000429994.5:c.214+216del	ENSP00000399422.1:n.214+216del
ENST00000494175.1:n.215+216del
NM_001308069.1:c.214+216del	NP_001294998.1:n.214+216del
NM_152531.4:c.652+216del	NP_689744.3:n.652+216del
XM_005269285.2:c.91+216del	XP_005269342.1:n.91+216del
XM_005269286.3:c.91+216del	XP_005269343.1:n.91+216del
XM_005269288.2:c.91+216del	XP_005269345.1:n.91+216del
XM_006713511.2:c.91+216del	XP_006713574.1:n.91+216del
XM_011512448.1:c.91+216del	XP_011510750.1:n.91+216del
XM_011512449.1:c.-71+216del	XP_011510751.1:n.-71+216del
XR_924104.1:n.731+216del
XR_924105.1:n.731+216del
XM_005269286.5:c.91+216del	XP_005269343.1:n.91+216del
XM_011512448.3:c.91+216del	XP_011510750.1:n.91+216del
XM_017005749.2:c.652+216del	XP_016861238.1:n.652+216del
XR_924105.3:n.728+216del
NM_152531.5:c.652+216del MANE Select	NP_689744.3:n.652+216del
NM_001308069.2:c.214+216del	NP_001294998.1:n.214+216del