Canonical Allele Identifier: CA9750995

Gene: RNF24

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3934100G>T , CM000682.2:g.3934100G>T	GRCh38
NC_000020.10:g.3914747G>T , CM000682.1:g.3914747G>T	GRCh37
NC_000020.9:g.3862747G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001134337.3:c.410C>A MANE Select	NP_001127809.1:p.Pro137His
ENST00000358395.11:c.410C>A MANE Select	ENSP00000351166.6:p.Pro137His
NM_001134337.1:c.410C>A	NP_001127809.1:p.Pro137His
NM_001134337.2:c.410C>A	NP_001127809.1:p.Pro137His
NM_001134338.1:c.473C>A	NP_001127810.1:p.Pro158His
NM_001134338.2:c.473C>A	NP_001127810.1:p.Pro158His
NM_001134338.3:c.473C>A	NP_001127810.1:p.Pro158His
NM_001321749.1:c.410C>A	NP_001308678.1:p.Pro137His
NM_001321749.2:c.410C>A	NP_001308678.1:p.Pro137His
NM_007219.3:c.410C>A	NP_009150.1:p.Pro137His
NM_007219.4:c.410C>A	NP_009150.1:p.Pro137His
NM_007219.5:c.410C>A	NP_009150.1:p.Pro137His
ENST00000336095.10:c.410C>A	ENSP00000336753.5:p.Pro137His
ENST00000358395.10:c.410C>A	ENSP00000351166.6:p.Pro137His
ENST00000432261.6:c.473C>A	ENSP00000388550.2:p.Pro158His
ENST00000545616.2:c.473C>A	ENSP00000444711.1:p.Pro158His
XM_006723536.2:c.410C>A	XP_006723599.1:p.Pro137His
XM_011529145.1:c.473C>A	XP_011527447.1:p.Pro158His
XM_011529145.3:c.473C>A	XP_011527447.1:p.Pro158His
XM_011529146.1:c.455C>A	XP_011527448.1:p.Pro152His
XM_011529146.2:c.455C>A	XP_011527448.1:p.Pro152His
XM_017027620.1:c.473C>A	XP_016883109.1:p.Pro158His
XM_017027621.1:c.473C>A	XP_016883110.1:p.Pro158His
XM_017027622.2:c.*277C>A	XP_016883111.1:n.*277C>A