Canonical Allele Identifier: CA2830535041

Gene: C4orf33

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.129109763A>C , CM000666.2:g.129109763A>C	GRCh38
NC_000004.11:g.130030918A>C , CM000666.1:g.130030918A>C	GRCh37
NC_000004.10:g.130250368A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425929.6:c.494+91A>C MANE Select	ENSP00000401090.1:n.494+91A>C
ENST00000281146.9:c.494+91A>C	ENSP00000281146.4:n.494+91A>C
ENST00000425929.5:c.494+91A>C	ENSP00000401090.1:n.494+91A>C
ENST00000502887.5:c.*87A>C	ENSP00000427406.1:n.*87A>C
NM_001099783.1:c.494+91A>C	NP_001093253.1:n.494+91A>C
NM_173487.2:c.494+91A>C	NP_775758.2:n.494+91A>C
XM_005262734.3:c.494+91A>C	XP_005262791.1:n.494+91A>C
XM_005262735.3:c.494+91A>C	XP_005262792.1:n.494+91A>C
XM_011531594.1:c.494+91A>C	XP_011529896.1:n.494+91A>C
XR_938690.1:n.556+91A>C
XM_005262734.5:c.494+91A>C	XP_005262791.1:n.494+91A>C
XM_017007722.1:c.521+91A>C	XP_016863211.1:n.521+91A>C
XM_017007723.1:c.521+91A>C	XP_016863212.1:n.521+91A>C
XM_017007724.1:c.494+91A>C	XP_016863213.1:n.494+91A>C
XR_001741132.1:n.1879+91A>C
NM_001099783.2:c.494+91A>C MANE Select	NP_001093253.1:n.494+91A>C
NM_173487.3:c.494+91A>C	NP_775758.2:n.494+91A>C