Canonical Allele Identifier: CA2631987662

Gene: XYLT1

Linked Data

• gnomAD v4: 16-17138781-C-CTGTTA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138782_17138783insGTTAT , CM000678.2:g.17138782_17138783insGTTAT	GRCh38
NC_000016.9:g.17232639_17232640insGTTAT , CM000678.1:g.17232639_17232640insGTTAT	GRCh37
NC_000016.8:g.17140140_17140141insGTTAT	NCBI36
NG_015843.1:g.337100_337101insTAACA
NG_015843.2:g.337100_337101insTAACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-251_1588-250insTAACA MANE Select	ENSP00000261381.6:n.1588-251_1588-250insTAACA
ENST00000261381.6:c.1588-251_1588-250insTAACA	ENSP00000261381.6:n.1588-251_1588-250insTAACA
NM_022166.3:c.1588-251_1588-250insTAACA	NP_071449.1:n.1588-251_1588-250insTAACA
XM_011522574.1:c.1588-251_1588-250insTAACA	XP_011520876.1:n.1588-251_1588-250insTAACA
XM_017023539.2:c.1588-251_1588-250insTAACA	XP_016879028.1:n.1588-251_1588-250insTAACA
XM_017023540.2:c.1588-251_1588-250insTAACA	XP_016879029.1:n.1588-251_1588-250insTAACA
NM_022166.4:c.1588-251_1588-250insTAACA MANE Select	NP_071449.1:n.1588-251_1588-250insTAACA