Canonical Allele Identifier: CA2210542143

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138511_17138527delinsCAGGACCGTATGGAAGA , CM000678.2:g.17138511_17138527delinsCAGGACCGTATGGAAGA	GRCh38
NC_000016.9:g.17232368_17232384delinsCAGGACCGTATGGAAGA , CM000678.1:g.17232368_17232384delinsCAGGACCGTATGGAAGA	GRCh37
NC_000016.8:g.17139869_17139885delinsCAGGACCGTATGGAAGA	NCBI36
NG_015843.1:g.337355_337371delinsTCTTCCATACGGTCCTG
NG_015843.2:g.337355_337371delinsTCTTCCATACGGTCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1592_1608delinsTCTTCCATACGGTCCTG MANE Select	ENSP00000261381.6:p.Phe531=
ENST00000261381.6:c.1592_1608delinsTCTTCCATACGGTCCTG	ENSP00000261381.6:p.Phe531=
NM_022166.3:c.1592_1608delinsTCTTCCATACGGTCCTG	NP_071449.1:p.Phe531=
XM_011522574.1:c.1592_1608delinsTCTTCCATACGGTCCTG	XP_011520876.1:p.Phe531=
XR_933141.1:n.444_460delinsCAGGACCGTATGGAAGA
NR_135179.1:n.416_432delinsCAGGACCGTATGGAAGA
XM_017023539.2:c.1592_1608delinsTCTTCCATACGGTCCTG	XP_016879028.1:p.Phe531=
XM_017023540.2:c.1592_1608delinsTCTTCCATACGGTCCTG	XP_016879029.1:p.Phe531=
NM_022166.4:c.1592_1608delinsTCTTCCATACGGTCCTG MANE Select	NP_071449.1:p.Phe531=