Canonical Allele Identifier: CA358133174

Gene: INTU

Linked Data

• MyVariant Identifiers: chr4:g.128564796G>T (hg19) ; chr4:g.127643641G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.127643641G>T , CM000666.2:g.127643641G>T	GRCh38
NC_000004.11:g.128564796G>T , CM000666.1:g.128564796G>T	GRCh37
NC_000004.10:g.128784246G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335251.11:c.267G>T MANE Select	ENSP00000334003.5:p.Arg89Ser
ENST00000335251.10:c.267G>T	ENSP00000334003.5:p.Arg89Ser
ENST00000503626.5:c.267G>T	ENSP00000426287.1:p.Arg89Ser
ENST00000503952.5:c.267G>T	ENSP00000421995.1:p.Arg89Ser
ENST00000504491.1:c.210G>T	ENSP00000422550.1:p.Arg70Ser
NM_015693.3:c.267G>T	NP_056508.2:p.Arg89Ser
XM_011531844.1:c.267G>T	XP_011530146.1:p.Arg89Ser
XM_011531845.1:c.267G>T	XP_011530147.1:p.Arg89Ser
XM_011531846.1:c.210G>T	XP_011530148.1:p.Arg70Ser
XM_011531849.1:c.267G>T	XP_011530151.1:p.Arg89Ser
XM_011531850.1:c.267G>T	XP_011530152.1:p.Arg89Ser
XM_011531851.1:c.267G>T	XP_011530153.1:p.Arg89Ser
XR_938720.1:n.370G>T
XM_011531844.3:c.267G>T	XP_011530146.1:p.Arg89Ser
XM_011531845.3:c.267G>T	XP_011530147.1:p.Arg89Ser
XM_011531849.3:c.267G>T	XP_011530151.1:p.Arg89Ser
XM_011531850.3:c.267G>T	XP_011530152.1:p.Arg89Ser
XM_011531851.3:c.267G>T	XP_011530153.1:p.Arg89Ser
XM_017008026.2:c.267G>T	XP_016863515.1:p.Arg89Ser
XR_001741201.1:n.342G>T
NM_015693.4:c.267G>T MANE Select	NP_056508.2:p.Arg89Ser