Canonical Allele Identifier: CA2210538923

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134903_17134915delinsTATAATAAGGGTG , CM000678.2:g.17134903_17134915delinsTATAATAAGGGTG	GRCh38
NC_000016.9:g.17228760_17228772delinsTATAATAAGGGTG , CM000678.1:g.17228760_17228772delinsTATAATAAGGGTG	GRCh37
NC_000016.8:g.17136261_17136273delinsTATAATAAGGGTG	NCBI36
NG_015843.1:g.340967_340979delinsCACCCTTATTATA
NG_015843.2:g.340967_340979delinsCACCCTTATTATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1765-180_1765-168delinsCACCCTTATTATA MANE Select	ENSP00000261381.6:n.1765-180_1765-168delinsCACCCTTATTATA
ENST00000261381.6:c.1765-180_1765-168delinsCACCCTTATTATA	ENSP00000261381.6:n.1765-180_1765-168delinsCACCCTTATTATA
NM_022166.3:c.1765-180_1765-168delinsCACCCTTATTATA	NP_071449.1:n.1765-180_1765-168delinsCACCCTTATTATA
XM_011522574.1:c.1765-180_1765-168delinsCACCCTTATTATA	XP_011520876.1:n.1765-180_1765-168delinsCACCCTTATTATA
XR_933140.1:n.82+353_82+365delinsTATAATAAGGGTG
XR_933141.1:n.75+353_75+365delinsTATAATAAGGGTG
XR_933143.1:n.82+353_82+365delinsTATAATAAGGGTG
NR_135179.1:n.47+353_47+365delinsTATAATAAGGGTG
XM_017023539.2:c.1765-180_1765-168delinsCACCCTTATTATA	XP_016879028.1:n.1765-180_1765-168delinsCACCCTTATTATA
XM_017023540.2:c.1765-180_1765-168delinsCACCCTTATTATA	XP_016879029.1:n.1765-180_1765-168delinsCACCCTTATTATA
NM_022166.4:c.1765-180_1765-168delinsCACCCTTATTATA MANE Select	NP_071449.1:n.1765-180_1765-168delinsCACCCTTATTATA