Canonical Allele Identifier: CA2631987383

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138186-T-TAAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138186_17138187insAAGG , CM000678.2:g.17138186_17138187insAAGG	GRCh38
NC_000016.9:g.17232043_17232044insAAGG , CM000678.1:g.17232043_17232044insAAGG	GRCh37
NC_000016.8:g.17139544_17139545insAAGG	NCBI36
NG_015843.1:g.337695_337696insCCTT
NG_015843.2:g.337695_337696insCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+168_1764+169insCCTT MANE Select	ENSP00000261381.6:n.1764+168_1764+169insCCTT
ENST00000261381.6:c.1764+168_1764+169insCCTT	ENSP00000261381.6:n.1764+168_1764+169insCCTT
NM_022166.3:c.1764+168_1764+169insCCTT	NP_071449.1:n.1764+168_1764+169insCCTT
XM_011522574.1:c.1764+168_1764+169insCCTT	XP_011520876.1:n.1764+168_1764+169insCCTT
XR_933140.1:n.336-56_336-55insAAGG
XR_933141.1:n.175-56_175-55insAAGG
XR_933143.1:n.237-56_237-55insAAGG
NR_135179.1:n.147-56_147-55insAAGG
XM_017023539.2:c.1764+168_1764+169insCCTT	XP_016879028.1:n.1764+168_1764+169insCCTT
XM_017023540.2:c.1764+168_1764+169insCCTT	XP_016879029.1:n.1764+168_1764+169insCCTT
NM_022166.4:c.1764+168_1764+169insCCTT MANE Select	NP_071449.1:n.1764+168_1764+169insCCTT