Canonical Allele Identifier: CA2631987498

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138239-C-CAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138240_17138241insATA , CM000678.2:g.17138240_17138241insATA	GRCh38
NC_000016.9:g.17232097_17232098insATA , CM000678.1:g.17232097_17232098insATA	GRCh37
NC_000016.8:g.17139598_17139599insATA	NCBI36
NG_015843.1:g.337642_337643insATT
NG_015843.2:g.337642_337643insATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+115_1764+116insATT MANE Select	ENSP00000261381.6:n.1764+115_1764+116insATT
ENST00000261381.6:c.1764+115_1764+116insATT	ENSP00000261381.6:n.1764+115_1764+116insATT
NM_022166.3:c.1764+115_1764+116insATT	NP_071449.1:n.1764+115_1764+116insATT
XM_011522574.1:c.1764+115_1764+116insATT	XP_011520876.1:n.1764+115_1764+116insATT
XR_933140.1:n.336-2_336-1insATA
XR_933141.1:n.175-2_175-1insATA
XR_933143.1:n.237-2_237-1insATA
NR_135179.1:n.147-2_147-1insATA
XM_017023539.2:c.1764+115_1764+116insATT	XP_016879028.1:n.1764+115_1764+116insATT
XM_017023540.2:c.1764+115_1764+116insATT	XP_016879029.1:n.1764+115_1764+116insATT
NM_022166.4:c.1764+115_1764+116insATT MANE Select	NP_071449.1:n.1764+115_1764+116insATT