Canonical Allele Identifier: CA919667544

Gene: XYLT1

Linked Data

• dbSNP Id: rs1567291173
• gnomAD v4: 16-17138229-TAATTATC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138232_17138238del , CM000678.2:g.17138232_17138238del	GRCh38
NC_000016.9:g.17232089_17232095del , CM000678.1:g.17232089_17232095del	GRCh37
NC_000016.8:g.17139590_17139596del	NCBI36
NG_015843.1:g.337646_337652del
NG_015843.2:g.337646_337652del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+119_1764+125del MANE Select	ENSP00000261381.6:n.1764+119_1764+125del
ENST00000261381.6:c.1764+119_1764+125del	ENSP00000261381.6:n.1764+119_1764+125del
NM_022166.3:c.1764+119_1764+125del	NP_071449.1:n.1764+119_1764+125del
XM_011522574.1:c.1764+119_1764+125del	XP_011520876.1:n.1764+119_1764+125del
XR_933140.1:n.336-10_336-4del
XR_933141.1:n.175-10_175-4del
XR_933143.1:n.237-10_237-4del
NR_135179.1:n.147-10_147-4del
XM_017023539.2:c.1764+119_1764+125del	XP_016879028.1:n.1764+119_1764+125del
XM_017023540.2:c.1764+119_1764+125del	XP_016879029.1:n.1764+119_1764+125del
NM_022166.4:c.1764+119_1764+125del MANE Select	NP_071449.1:n.1764+119_1764+125del