Canonical Allele Identifier: CA2210541601

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138229_17138230delinsTA , CM000678.2:g.17138229_17138230delinsTA	GRCh38
NC_000016.9:g.17232086_17232087delinsTA , CM000678.1:g.17232086_17232087delinsTA	GRCh37
NC_000016.8:g.17139587_17139588delinsTA	NCBI36
NG_015843.1:g.337652_337653delinsTA
NG_015843.2:g.337652_337653delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+125_1764+126delinsTA MANE Select	ENSP00000261381.6:n.1764+125_1764+126delinsTA
ENST00000261381.6:c.1764+125_1764+126delinsTA	ENSP00000261381.6:n.1764+125_1764+126delinsTA
NM_022166.3:c.1764+125_1764+126delinsTA	NP_071449.1:n.1764+125_1764+126delinsTA
XM_011522574.1:c.1764+125_1764+126delinsTA	XP_011520876.1:n.1764+125_1764+126delinsTA
XR_933140.1:n.336-13_336-12delinsTA
XR_933141.1:n.175-13_175-12delinsTA
XR_933143.1:n.237-13_237-12delinsTA
NR_135179.1:n.147-13_147-12delinsTA
XM_017023539.2:c.1764+125_1764+126delinsTA	XP_016879028.1:n.1764+125_1764+126delinsTA
XM_017023540.2:c.1764+125_1764+126delinsTA	XP_016879029.1:n.1764+125_1764+126delinsTA
NM_022166.4:c.1764+125_1764+126delinsTA MANE Select	NP_071449.1:n.1764+125_1764+126delinsTA