Canonical Allele Identifier: CA2210538916

Gene: XYLT1

Linked Data

• dbSNP Id: rs2030652070
• gnomAD v4: 16-17134886-A-ACAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17134888_17134890dup , CM000678.2:g.17134888_17134890dup	GRCh38
NC_000016.9:g.17228745_17228747dup , CM000678.1:g.17228745_17228747dup	GRCh37
NC_000016.8:g.17136246_17136248dup	NCBI36
NG_015843.1:g.340993_340995dup
NG_015843.2:g.340993_340995dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1765-154_1765-152dup MANE Select	ENSP00000261381.6:n.1765-154_1765-152dup
ENST00000261381.6:c.1765-154_1765-152dup	ENSP00000261381.6:n.1765-154_1765-152dup
NM_022166.3:c.1765-154_1765-152dup	NP_071449.1:n.1765-154_1765-152dup
XM_011522574.1:c.1765-154_1765-152dup	XP_011520876.1:n.1765-154_1765-152dup
XR_933140.1:n.82+338_82+340dup
XR_933141.1:n.75+338_75+340dup
XR_933143.1:n.82+338_82+340dup
NR_135179.1:n.47+338_47+340dup
XM_017023539.2:c.1765-154_1765-152dup	XP_016879028.1:n.1765-154_1765-152dup
XM_017023540.2:c.1765-154_1765-152dup	XP_016879029.1:n.1765-154_1765-152dup
NM_022166.4:c.1765-154_1765-152dup MANE Select	NP_071449.1:n.1765-154_1765-152dup