Canonical Allele Identifier: CA1980136680

Gene: CABP4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67456201_67456202delinsGC , CM000673.2:g.67456201_67456202delinsGC	GRCh38
NC_000011.9:g.67223672_67223673delinsGC , CM000673.1:g.67223672_67223673delinsGC	GRCh37
NC_000011.8:g.66980248_66980249delinsGC	NCBI36
NG_021211.1:g.5855_5856delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000325656.7:c.380_381delinsGC MANE Select	ENSP00000324960.5:p.Gly127=
ENST00000325656.6:c.380_381delinsGC	ENSP00000324960.5:p.Gly127=
ENST00000438189.6:c.65_66delinsGC	ENSP00000401555.2:p.Gly22=
ENST00000545777.1:c.*61_*62delinsGC	ENSP00000439145.1:n.*61_*62delinsGC
NM_001300895.1:c.65_66delinsGC	NP_001287824.1:p.Gly22=
NM_001300896.1:c.65_66delinsGC	NP_001287825.1:p.Gly22=
NM_145200.3:c.380_381delinsGC	NP_660201.1:p.Gly127=
XM_005274114.2:c.440_441delinsGC	XP_005274171.2:p.Gly147=
XM_011545181.1:c.440_441delinsGC	XP_011543483.1:p.Gly147=
XM_011545182.1:c.440_441delinsGC	XP_011543484.1:p.Gly147=
XM_011545183.1:c.65_66delinsGC	XP_011543485.1:p.Gly22=
XM_011545184.1:c.65_66delinsGC	XP_011543486.1:p.Gly22=
XM_005274114.3:c.440_441delinsGC	XP_005274171.2:p.Gly147=
XM_011545181.2:c.440_441delinsGC	XP_011543483.1:p.Gly147=
XM_011545182.2:c.440_441delinsGC	XP_011543484.1:p.Gly147=
XM_011545183.2:c.65_66delinsGC	XP_011543485.1:p.Gly22=
XM_017018025.1:c.65_66delinsGC	XP_016873514.1:p.Gly22=
XM_024448615.1:c.380_381delinsGC	XP_024304383.1:p.Gly127=
XM_024448616.1:c.65_66delinsGC	XP_024304384.1:p.Gly22=
NM_001300895.2:c.65_66delinsGC	NP_001287824.1:p.Gly22=
NM_001300896.2:c.65_66delinsGC	NP_001287825.1:p.Gly22=
NM_145200.4:c.380_381delinsGC	NP_660201.1:p.Gly127=
NM_001300895.3:c.65_66delinsGC	NP_001287824.1:p.Gly22=
NM_001300896.3:c.65_66delinsGC	NP_001287825.1:p.Gly22=
NM_001379183.1:c.65_66delinsGC	NP_001366112.1:p.Gly22=
NM_145200.5:c.380_381delinsGC MANE Select	NP_660201.1:p.Gly127=
NR_166529.1:n.436+412_436+413delinsGC