Canonical Allele Identifier: CA2806078114

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138186_17138187insAACT , CM000678.2:g.17138186_17138187insAACT	GRCh38
NC_000016.9:g.17232043_17232044insAACT , CM000678.1:g.17232043_17232044insAACT	GRCh37
NC_000016.8:g.17139544_17139545insAACT	NCBI36
NG_015843.1:g.337696_337697insGTTA
NG_015843.2:g.337696_337697insGTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+169_1764+170insGTTA MANE Select	ENSP00000261381.6:n.1764+169_1764+170insGTTA
ENST00000261381.6:c.1764+169_1764+170insGTTA	ENSP00000261381.6:n.1764+169_1764+170insGTTA
NM_022166.3:c.1764+169_1764+170insGTTA	NP_071449.1:n.1764+169_1764+170insGTTA
XM_011522574.1:c.1764+169_1764+170insGTTA	XP_011520876.1:n.1764+169_1764+170insGTTA
XR_933140.1:n.336-56_336-55insAACT
XR_933141.1:n.175-56_175-55insAACT
XR_933143.1:n.237-56_237-55insAACT
NR_135179.1:n.147-56_147-55insAACT
XM_017023539.2:c.1764+169_1764+170insGTTA	XP_016879028.1:n.1764+169_1764+170insGTTA
XM_017023540.2:c.1764+169_1764+170insGTTA	XP_016879029.1:n.1764+169_1764+170insGTTA
NM_022166.4:c.1764+169_1764+170insGTTA MANE Select	NP_071449.1:n.1764+169_1764+170insGTTA