Canonical Allele Identifier: CA2104657

Gene: CATIP CATIP-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218367894G>A , CM000664.2:g.218367894G>A	GRCh38
NC_000002.11:g.219232617G>A , CM000664.1:g.219232617G>A	GRCh37
NC_000002.10:g.218940861G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289388.4:c.1094G>A (CATIP) MANE Select	ENSP00000289388.3:p.Gly365Asp
ENST00000289388.3:c.1094G>A (CATIP)	ENSP00000289388.3:p.Gly365Asp
ENST00000481940.1:n.565G>A (CATIP)
ENST00000494447.1:n.2184G>A (CATIP)
NM_198559.1:c.1094G>A (CATIP)	NP_940961.1:p.Gly365Asp
NR_110573.1:n.9C>T (CATIP-AS1)
XM_005246539.3:c.1001G>A (CATIP)	XP_005246596.1:p.Gly334Asp
XM_005246541.3:c.800G>A (CATIP)	XP_005246598.1:p.Gly267Asp
XM_011511147.1:c.1127G>A (CATIP)	XP_011509449.1:p.Gly376Asp
XM_011511148.1:c.959G>A (CATIP)	XP_011509450.1:p.Gly320Asp
XM_011511149.1:c.749G>A (CATIP)	XP_011509451.1:p.Gly250Asp
XM_011511150.1:c.749G>A (CATIP)	XP_011509452.1:p.Gly250Asp
NM_001320865.1:c.1127G>A (CATIP)	NP_001307794.1:p.Gly376Asp
XM_005246539.4:c.1001G>A (CATIP)	XP_005246596.1:p.Gly334Asp
XM_005246541.4:c.800G>A (CATIP)	XP_005246598.1:p.Gly267Asp
XM_011511148.2:c.959G>A (CATIP)	XP_011509450.1:p.Gly320Asp
XM_011511149.2:c.749G>A (CATIP)	XP_011509451.1:p.Gly250Asp
XM_011511150.2:c.749G>A (CATIP)	XP_011509452.1:p.Gly250Asp
XM_017004053.2:c.545G>A (CATIP)	XP_016859542.1:p.Gly182Asp
NM_198559.2:c.1094G>A (CATIP) MANE Select	NP_940961.1:p.Gly365Asp
NM_001320865.2:c.1127G>A (CATIP)	NP_001307794.1:p.Gly376Asp