Canonical Allele Identifier: CA2210542255

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138564_17138572delinsTCTCCCAGC , CM000678.2:g.17138564_17138572delinsTCTCCCAGC	GRCh38
NC_000016.9:g.17232421_17232429delinsTCTCCCAGC , CM000678.1:g.17232421_17232429delinsTCTCCCAGC	GRCh37
NC_000016.8:g.17139922_17139930delinsTCTCCCAGC	NCBI36
NG_015843.1:g.337310_337318delinsGCTGGGAGA
NG_015843.2:g.337310_337318delinsGCTGGGAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-41_1588-33delinsGCTGGGAGA MANE Select	ENSP00000261381.6:n.1588-41_1588-33delinsGCTGGGAGA
ENST00000261381.6:c.1588-41_1588-33delinsGCTGGGAGA	ENSP00000261381.6:n.1588-41_1588-33delinsGCTGGGAGA
NM_022166.3:c.1588-41_1588-33delinsGCTGGGAGA	NP_071449.1:n.1588-41_1588-33delinsGCTGGGAGA
XM_011522574.1:c.1588-41_1588-33delinsGCTGGGAGA	XP_011520876.1:n.1588-41_1588-33delinsGCTGGGAGA
XR_933141.1:n.497_505delinsTCTCCCAGC
NR_135179.1:n.469_477delinsTCTCCCAGC
XM_017023539.2:c.1588-41_1588-33delinsGCTGGGAGA	XP_016879028.1:n.1588-41_1588-33delinsGCTGGGAGA
XM_017023540.2:c.1588-41_1588-33delinsGCTGGGAGA	XP_016879029.1:n.1588-41_1588-33delinsGCTGGGAGA
NM_022166.4:c.1588-41_1588-33delinsGCTGGGAGA MANE Select	NP_071449.1:n.1588-41_1588-33delinsGCTGGGAGA