Canonical Allele Identifier: CA2210542711

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138784_17138788delinsCCTGA , CM000678.2:g.17138784_17138788delinsCCTGA	GRCh38
NC_000016.9:g.17232641_17232645delinsCCTGA , CM000678.1:g.17232641_17232645delinsCCTGA	GRCh37
NC_000016.8:g.17140142_17140146delinsCCTGA	NCBI36
NG_015843.1:g.337094_337098delinsTCAGG
NG_015843.2:g.337094_337098delinsTCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-257_1588-253delinsTCAGG MANE Select	ENSP00000261381.6:n.1588-257_1588-253delinsTCAGG
ENST00000261381.6:c.1588-257_1588-253delinsTCAGG	ENSP00000261381.6:n.1588-257_1588-253delinsTCAGG
NM_022166.3:c.1588-257_1588-253delinsTCAGG	NP_071449.1:n.1588-257_1588-253delinsTCAGG
XM_011522574.1:c.1588-257_1588-253delinsTCAGG	XP_011520876.1:n.1588-257_1588-253delinsTCAGG
XM_017023539.2:c.1588-257_1588-253delinsTCAGG	XP_016879028.1:n.1588-257_1588-253delinsTCAGG
XM_017023540.2:c.1588-257_1588-253delinsTCAGG	XP_016879029.1:n.1588-257_1588-253delinsTCAGG
NM_022166.4:c.1588-257_1588-253delinsTCAGG MANE Select	NP_071449.1:n.1588-257_1588-253delinsTCAGG