Canonical Allele Identifier: CA382489571

Gene: CFAP300

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102075915C>T , CM000673.2:g.102075915C>T	GRCh38
NC_000011.9:g.101946646C>T , CM000673.1:g.101946646C>T	GRCh37
NC_000011.8:g.101451856C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_032930.3:c.478C>T MANE Select	NP_116319.2:p.Gln160Ter
ENST00000434758.7:c.478C>T MANE Select	ENSP00000414390.2:p.Gln160Ter
NM_001195005.1:c.*11C>T	NP_001181934.1:n.*11C>T
NM_001195005.2:c.*11C>T	NP_001181934.1:n.*11C>T
NM_001363505.1:c.478C>T	NP_001350434.1:p.Gln160Ter
NM_001363505.2:c.478C>T	NP_001350434.1:p.Gln160Ter
NM_032930.2:c.478C>T	NP_116319.2:p.Gln160Ter
ENST00000434758.6:c.478C>T	ENSP00000414390.2:p.Gln160Ter
ENST00000526781.5:c.478C>T	ENSP00000433074.1:p.Gln160Ter
ENST00000529204.1:c.153C>T
ENST00000530659.1:n.715C>T
ENST00000534360.1:c.*11C>T	ENSP00000435482.1:n.*11C>T
XM_005271713.2:c.478C>T	XP_005271770.1:p.Gln160Ter
XM_005271713.4:c.478C>T	XP_005271770.1:p.Gln160Ter
XM_006718929.2:c.269-5300C>T	XP_006718992.1:n.269-5300C>T
XM_017018454.1:c.436-5300C>T	XP_016873943.1:n.436-5300C>T