Canonical Allele Identifier: CA2104638

Gene: CATIP CATIP-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218367842G>A , CM000664.2:g.218367842G>A	GRCh38
NC_000002.11:g.219232565G>A , CM000664.1:g.219232565G>A	GRCh37
NC_000002.10:g.218940809G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289388.4:c.1042G>A (CATIP) MANE Select	ENSP00000289388.3:p.Ala348Thr
ENST00000289388.3:c.1042G>A (CATIP)	ENSP00000289388.3:p.Ala348Thr
ENST00000481940.1:n.513G>A (CATIP)
ENST00000494447.1:n.2132G>A (CATIP)
NM_198559.1:c.1042G>A (CATIP)	NP_940961.1:p.Ala348Thr
NR_110573.1:n.61C>T (CATIP-AS1)
XM_005246539.3:c.949G>A (CATIP)	XP_005246596.1:p.Ala317Thr
XM_005246541.3:c.748G>A (CATIP)	XP_005246598.1:p.Ala250Thr
XM_011511147.1:c.1075G>A (CATIP)	XP_011509449.1:p.Ala359Thr
XM_011511148.1:c.907G>A (CATIP)	XP_011509450.1:p.Ala303Thr
XM_011511149.1:c.697G>A (CATIP)	XP_011509451.1:p.Ala233Thr
XM_011511150.1:c.697G>A (CATIP)	XP_011509452.1:p.Ala233Thr
NM_001320865.1:c.1075G>A (CATIP)	NP_001307794.1:p.Ala359Thr
XM_005246539.4:c.949G>A (CATIP)	XP_005246596.1:p.Ala317Thr
XM_005246541.4:c.748G>A (CATIP)	XP_005246598.1:p.Ala250Thr
XM_011511148.2:c.907G>A (CATIP)	XP_011509450.1:p.Ala303Thr
XM_011511149.2:c.697G>A (CATIP)	XP_011509451.1:p.Ala233Thr
XM_011511150.2:c.697G>A (CATIP)	XP_011509452.1:p.Ala233Thr
XM_017004053.2:c.493G>A (CATIP)	XP_016859542.1:p.Ala165Thr
NM_198559.2:c.1042G>A (CATIP) MANE Select	NP_940961.1:p.Ala348Thr
NM_001320865.2:c.1075G>A (CATIP)	NP_001307794.1:p.Ala359Thr