Canonical Allele Identifier: CA2631987280

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138160-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138160T>A , CM000678.2:g.17138160T>A	GRCh38
NC_000016.9:g.17232017T>A , CM000678.1:g.17232017T>A	GRCh37
NC_000016.8:g.17139518T>A	NCBI36
NG_015843.1:g.337722A>T
NG_015843.2:g.337722A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+195A>T MANE Select	ENSP00000261381.6:n.1764+195A>T
ENST00000261381.6:c.1764+195A>T	ENSP00000261381.6:n.1764+195A>T
NM_022166.3:c.1764+195A>T	NP_071449.1:n.1764+195A>T
XM_011522574.1:c.1764+195A>T	XP_011520876.1:n.1764+195A>T
XR_933140.1:n.336-82T>A
XR_933141.1:n.175-82T>A
XR_933143.1:n.237-82T>A
NR_135179.1:n.147-82T>A
XM_017023539.2:c.1764+195A>T	XP_016879028.1:n.1764+195A>T
XM_017023540.2:c.1764+195A>T	XP_016879029.1:n.1764+195A>T
NM_022166.4:c.1764+195A>T MANE Select	NP_071449.1:n.1764+195A>T