Canonical Allele Identifier: CA2631987373

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138184-A-ACATCCCTGAAATAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138184_17138185insCATCCCTGAAATAT , CM000678.2:g.17138184_17138185insCATCCCTGAAATAT	GRCh38
NC_000016.9:g.17232041_17232042insCATCCCTGAAATAT , CM000678.1:g.17232041_17232042insCATCCCTGAAATAT	GRCh37
NC_000016.8:g.17139542_17139543insCATCCCTGAAATAT	NCBI36
NG_015843.1:g.337697_337698insATATTTCAGGGATG
NG_015843.2:g.337697_337698insATATTTCAGGGATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+170_1764+171insATATTTCAGGGATG MANE Select	ENSP00000261381.6:n.1764+170_1764+171insATATTTCAGGGATG
ENST00000261381.6:c.1764+170_1764+171insATATTTCAGGGATG	ENSP00000261381.6:n.1764+170_1764+171insATATTTCAGGGATG
NM_022166.3:c.1764+170_1764+171insATATTTCAGGGATG	NP_071449.1:n.1764+170_1764+171insATATTTCAGGGATG
XM_011522574.1:c.1764+170_1764+171insATATTTCAGGGATG	XP_011520876.1:n.1764+170_1764+171insATATTTCAGGGATG
XR_933140.1:n.336-58_336-57insCATCCCTGAAATAT
XR_933141.1:n.175-58_175-57insCATCCCTGAAATAT
XR_933143.1:n.237-58_237-57insCATCCCTGAAATAT
NR_135179.1:n.147-58_147-57insCATCCCTGAAATAT
XM_017023539.2:c.1764+170_1764+171insATATTTCAGGGATG	XP_016879028.1:n.1764+170_1764+171insATATTTCAGGGATG
XM_017023540.2:c.1764+170_1764+171insATATTTCAGGGATG	XP_016879029.1:n.1764+170_1764+171insATATTTCAGGGATG
NM_022166.4:c.1764+170_1764+171insATATTTCAGGGATG MANE Select	NP_071449.1:n.1764+170_1764+171insATATTTCAGGGATG