Canonical Allele Identifier: CA2210541421

Gene: XYLT1

Linked Data

• dbSNP Id: rs2030818097
• gnomAD v4: 16-17138103-T-TCCCTAAAATGGAATAATAA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138104_17138122dup , CM000678.2:g.17138104_17138122dup	GRCh38
NC_000016.9:g.17231961_17231979dup , CM000678.1:g.17231961_17231979dup	GRCh37
NC_000016.8:g.17139462_17139480dup	NCBI36
NG_015843.1:g.337760_337778dup
NG_015843.2:g.337760_337778dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+233_1764+251dup MANE Select	ENSP00000261381.6:n.1764+233_1764+251dup
ENST00000261381.6:c.1764+233_1764+251dup	ENSP00000261381.6:n.1764+233_1764+251dup
NM_022166.3:c.1764+233_1764+251dup	NP_071449.1:n.1764+233_1764+251dup
XM_011522574.1:c.1764+233_1764+251dup	XP_011520876.1:n.1764+233_1764+251dup
XR_933140.1:n.336-138_336-120dup
XR_933141.1:n.175-138_175-120dup
XR_933143.1:n.237-138_237-120dup
NR_135179.1:n.147-138_147-120dup
XM_017023539.2:c.1764+233_1764+251dup	XP_016879028.1:n.1764+233_1764+251dup
XM_017023540.2:c.1764+233_1764+251dup	XP_016879029.1:n.1764+233_1764+251dup
NM_022166.4:c.1764+233_1764+251dup MANE Select	NP_071449.1:n.1764+233_1764+251dup