Canonical Allele Identifier: CA2210541729

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138323_17138336delinsTAGGAGGCTGGCAG , CM000678.2:g.17138323_17138336delinsTAGGAGGCTGGCAG	GRCh38
NC_000016.9:g.17232180_17232193delinsTAGGAGGCTGGCAG , CM000678.1:g.17232180_17232193delinsTAGGAGGCTGGCAG	GRCh37
NC_000016.8:g.17139681_17139694delinsTAGGAGGCTGGCAG	NCBI36
NG_015843.1:g.337546_337559delinsCTGCCAGCCTCCTA
NG_015843.2:g.337546_337559delinsCTGCCAGCCTCCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+19_1764+32delinsCTGCCAGCCTCCTA MANE Select	ENSP00000261381.6:n.1764+19_1764+32delinsCTGCCAGCCTCCTA
ENST00000261381.6:c.1764+19_1764+32delinsCTGCCAGCCTCCTA	ENSP00000261381.6:n.1764+19_1764+32delinsCTGCCAGCCTCCTA
NM_022166.3:c.1764+19_1764+32delinsCTGCCAGCCTCCTA	NP_071449.1:n.1764+19_1764+32delinsCTGCCAGCCTCCTA
XM_011522574.1:c.1764+19_1764+32delinsCTGCCAGCCTCCTA	XP_011520876.1:n.1764+19_1764+32delinsCTGCCAGCCTCCTA
XR_933140.1:n.417_430delinsTAGGAGGCTGGCAG
XR_933141.1:n.256_269delinsTAGGAGGCTGGCAG
XR_933143.1:n.318_331delinsTAGGAGGCTGGCAG
NR_135179.1:n.228_241delinsTAGGAGGCTGGCAG
XM_017023539.2:c.1764+19_1764+32delinsCTGCCAGCCTCCTA	XP_016879028.1:n.1764+19_1764+32delinsCTGCCAGCCTCCTA
XM_017023540.2:c.1764+19_1764+32delinsCTGCCAGCCTCCTA	XP_016879029.1:n.1764+19_1764+32delinsCTGCCAGCCTCCTA
NM_022166.4:c.1764+19_1764+32delinsCTGCCAGCCTCCTA MANE Select	NP_071449.1:n.1764+19_1764+32delinsCTGCCAGCCTCCTA