Canonical Allele Identifier: CA2631987194

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138117-T-TAATAATG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138120_17138126dup , CM000678.2:g.17138120_17138126dup	GRCh38
NC_000016.9:g.17231977_17231983dup , CM000678.1:g.17231977_17231983dup	GRCh37
NC_000016.8:g.17139478_17139484dup	NCBI36
NG_015843.1:g.337758_337764dup
NG_015843.2:g.337758_337764dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+231_1764+237dup MANE Select	ENSP00000261381.6:n.1764+231_1764+237dup
ENST00000261381.6:c.1764+231_1764+237dup	ENSP00000261381.6:n.1764+231_1764+237dup
NM_022166.3:c.1764+231_1764+237dup	NP_071449.1:n.1764+231_1764+237dup
XM_011522574.1:c.1764+231_1764+237dup	XP_011520876.1:n.1764+231_1764+237dup
XR_933140.1:n.336-122_336-116dup
XR_933141.1:n.175-122_175-116dup
XR_933143.1:n.237-122_237-116dup
NR_135179.1:n.147-122_147-116dup
XM_017023539.2:c.1764+231_1764+237dup	XP_016879028.1:n.1764+231_1764+237dup
XM_017023540.2:c.1764+231_1764+237dup	XP_016879029.1:n.1764+231_1764+237dup
NM_022166.4:c.1764+231_1764+237dup MANE Select	NP_071449.1:n.1764+231_1764+237dup