Canonical Allele Identifier: CA2210541606

Gene: XYLT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138230_17138232delinsAAT , CM000678.2:g.17138230_17138232delinsAAT	GRCh38
NC_000016.9:g.17232087_17232089delinsAAT , CM000678.1:g.17232087_17232089delinsAAT	GRCh37
NC_000016.8:g.17139588_17139590delinsAAT	NCBI36
NG_015843.1:g.337650_337652delinsATT
NG_015843.2:g.337650_337652delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1764+123_1764+125delinsATT MANE Select	ENSP00000261381.6:n.1764+123_1764+125delinsATT
ENST00000261381.6:c.1764+123_1764+125delinsATT	ENSP00000261381.6:n.1764+123_1764+125delinsATT
NM_022166.3:c.1764+123_1764+125delinsATT	NP_071449.1:n.1764+123_1764+125delinsATT
XM_011522574.1:c.1764+123_1764+125delinsATT	XP_011520876.1:n.1764+123_1764+125delinsATT
XR_933140.1:n.336-12_336-10delinsAAT
XR_933141.1:n.175-12_175-10delinsAAT
XR_933143.1:n.237-12_237-10delinsAAT
NR_135179.1:n.147-12_147-10delinsAAT
XM_017023539.2:c.1764+123_1764+125delinsATT	XP_016879028.1:n.1764+123_1764+125delinsATT
XM_017023540.2:c.1764+123_1764+125delinsATT	XP_016879029.1:n.1764+123_1764+125delinsATT
NM_022166.4:c.1764+123_1764+125delinsATT MANE Select	NP_071449.1:n.1764+123_1764+125delinsATT