Canonical Allele Identifier: CA2806078124

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138535_17138536insTTCC , CM000678.2:g.17138535_17138536insTTCC	GRCh38
NC_000016.9:g.17232392_17232393insTTCC , CM000678.1:g.17232392_17232393insTTCC	GRCh37
NC_000016.8:g.17139893_17139894insTTCC	NCBI36
NG_015843.1:g.337347_337348insGAAG
NG_015843.2:g.337347_337348insGAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-4_1588-3insGAAG MANE Select	ENSP00000261381.6:n.1588-4_1588-3insGAAG
ENST00000261381.6:c.1588-4_1588-3insGAAG	ENSP00000261381.6:n.1588-4_1588-3insGAAG
NM_022166.3:c.1588-4_1588-3insGAAG	NP_071449.1:n.1588-4_1588-3insGAAG
XM_011522574.1:c.1588-4_1588-3insGAAG	XP_011520876.1:n.1588-4_1588-3insGAAG
XR_933141.1:n.468_469insTTCC
NR_135179.1:n.440_441insTTCC
XM_017023539.2:c.1588-4_1588-3insGAAG	XP_016879028.1:n.1588-4_1588-3insGAAG
XM_017023540.2:c.1588-4_1588-3insGAAG	XP_016879029.1:n.1588-4_1588-3insGAAG
NM_022166.4:c.1588-4_1588-3insGAAG MANE Select	NP_071449.1:n.1588-4_1588-3insGAAG