Canonical Allele Identifier: CA1492708190

Gene: INTU

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.127687723dup , CM000666.2:g.127687723dup	GRCh38
NC_000004.11:g.128608878dup , CM000666.1:g.128608878dup	GRCh37
NC_000004.10:g.128828328dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015693.4:c.1305dup MANE Select	NP_056508.2:p.Asn436Ter
ENST00000335251.11:c.1305dup MANE Select	ENSP00000334003.5:p.Asn436Ter
NM_015693.3:c.1305dup	NP_056508.2:p.Asn436Ter
ENST00000335251.10:c.1305dup	ENSP00000334003.5:p.Asn436Ter
ENST00000503626.5:c.*2572dup	ENSP00000426287.1:n.*2572dup
ENST00000503952.5:c.*80-18dup	ENSP00000421995.1:n.*80-18dup
XM_011531844.1:c.1302dup	XP_011530146.1:p.Asn435Ter
XM_011531844.3:c.1302dup	XP_011530146.1:p.Asn435Ter
XM_011531845.1:c.1305dup	XP_011530147.1:p.Asn436Ter
XM_011531845.3:c.1305dup	XP_011530147.1:p.Asn436Ter
XM_011531846.1:c.1248dup	XP_011530148.1:p.Asn417Ter
XM_011531847.1:c.309dup	XP_011530149.1:p.Asn104Ter
XM_011531848.1:c.99dup	XP_011530150.1:p.Asn34Ter
XM_011531848.2:c.99dup	XP_011530150.1:p.Asn34Ter
XM_011531849.1:c.1305dup	XP_011530151.1:p.Asn436Ter
XM_011531849.3:c.1305dup	XP_011530151.1:p.Asn436Ter
XM_011531850.1:c.1305dup	XP_011530152.1:p.Asn436Ter
XM_011531850.3:c.1305dup	XP_011530152.1:p.Asn436Ter
XM_011531851.1:c.1305dup	XP_011530153.1:p.Asn436Ter
XM_011531851.3:c.1305dup	XP_011530153.1:p.Asn436Ter
XM_017008025.1:c.309dup	XP_016863514.1:p.Asn104Ter
XM_017008026.2:c.1305dup	XP_016863515.1:p.Asn436Ter
XR_001741201.1:n.1380dup
XR_938720.1:n.1408dup