Canonical Allele Identifier: CA1546832200

Gene: ARL15

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.54005004_54005005delinsCT , CM000667.2:g.54005004_54005005delinsCT	GRCh38
NC_000005.9:g.53300834_53300835delinsCT , CM000667.1:g.53300834_53300835delinsCT	GRCh37
NC_000005.8:g.53336591_53336592delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504924.6:c.462+108197_462+108198delinsAG MANE Select	ENSP00000433427.1:n.462+108197_462+108198delinsAG
ENST00000502271.5:c.-76+108197_-76+108198delinsAG	ENSP00000473508.1:n.-76+108197_-76+108198delinsAG
ENST00000504924.5:c.462+108197_462+108198delinsAG	ENSP00000433427.1:n.462+108197_462+108198delinsAG
ENST00000507646.2:c.462+108197_462+108198delinsAG	ENSP00000432680.1:n.462+108197_462+108198delinsAG
ENST00000510591.6:n.535+108197_535+108198delinsAG
ENST00000620747.4:c.468+62157_468+62158delinsAG	ENSP00000478984.1:n.468+62157_468+62158delinsAG
NM_019087.2:c.462+108197_462+108198delinsAG	NP_061960.1:n.462+108197_462+108198delinsAG
XM_011543498.1:c.645+108197_645+108198delinsAG	XP_011541800.1:n.645+108197_645+108198delinsAG
XM_011543499.1:c.588+108197_588+108198delinsAG	XP_011541801.1:n.588+108197_588+108198delinsAG
XM_011543500.1:c.519+108197_519+108198delinsAG	XP_011541802.1:n.519+108197_519+108198delinsAG
XM_011543498.2:c.645+108197_645+108198delinsAG	XP_011541800.1:n.645+108197_645+108198delinsAG
XM_011543499.2:c.588+108197_588+108198delinsAG	XP_011541801.1:n.588+108197_588+108198delinsAG
XM_011543500.2:c.519+108197_519+108198delinsAG	XP_011541802.1:n.519+108197_519+108198delinsAG
XM_017009598.1:c.468+108197_468+108198delinsAG	XP_016865087.1:n.468+108197_468+108198delinsAG
NM_019087.3:c.462+108197_462+108198delinsAG MANE Select	NP_061960.1:n.462+108197_462+108198delinsAG