Canonical Allele Identifier: CA2631987625

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138733-C-CTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138733_17138734insTG , CM000678.2:g.17138733_17138734insTG	GRCh38
NC_000016.9:g.17232590_17232591insTG , CM000678.1:g.17232590_17232591insTG	GRCh37
NC_000016.8:g.17140091_17140092insTG	NCBI36
NG_015843.1:g.337148_337149insCA
NG_015843.2:g.337148_337149insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-203_1588-202insCA MANE Select	ENSP00000261381.6:n.1588-203_1588-202insCA
ENST00000261381.6:c.1588-203_1588-202insCA	ENSP00000261381.6:n.1588-203_1588-202insCA
NM_022166.3:c.1588-203_1588-202insCA	NP_071449.1:n.1588-203_1588-202insCA
XM_011522574.1:c.1588-203_1588-202insCA	XP_011520876.1:n.1588-203_1588-202insCA
XM_017023539.2:c.1588-203_1588-202insCA	XP_016879028.1:n.1588-203_1588-202insCA
XM_017023540.2:c.1588-203_1588-202insCA	XP_016879029.1:n.1588-203_1588-202insCA
NM_022166.4:c.1588-203_1588-202insCA MANE Select	NP_071449.1:n.1588-203_1588-202insCA