Canonical Allele Identifier: CA4827966

Gene: RNF19A SPAG1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.100259131C>T , CM000670.2:g.100259131C>T	GRCh38
NC_000008.10:g.101271359C>T , CM000670.1:g.101271359C>T	GRCh37
NC_000008.9:g.101340535C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_183419.4:c.1942G>A (RNF19A) MANE Select	NP_904355.1:p.Gly648Ser
ENST00000341084.7:c.1942G>A (RNF19A) MANE Select	ENSP00000342667.2:p.Gly648Ser
NM_001280539.1:c.1942G>A (RNF19A)	NP_001267468.1:p.Gly648Ser
NM_001280539.2:c.1942G>A (RNF19A)	NP_001267468.1:p.Gly648Ser
NM_001353837.1:c.1942G>A (RNF19A)	NP_001340766.1:p.Gly648Ser
NM_001353837.2:c.1942G>A (RNF19A)	NP_001340766.1:p.Gly648Ser
NM_001353838.1:c.1942G>A (RNF19A)	NP_001340767.1:p.Gly648Ser
NM_001353838.2:c.1942G>A (RNF19A)	NP_001340767.1:p.Gly648Ser
NM_015435.4:c.1942G>A (RNF19A)	NP_056250.3:p.Gly648Ser
NM_015435.5:c.1942G>A (RNF19A)	NP_056250.3:p.Gly648Ser
NM_183419.3:c.1942G>A (RNF19A)	NP_904355.1:p.Gly648Ser
ENST00000341084.6:c.1942G>A (RNF19A)	ENSP00000342667.2:p.Gly648Ser
ENST00000519409.1:n.303C>T (SPAG1)
ENST00000519449.5:c.1942G>A (RNF19A)	ENSP00000428968.1:p.Gly648Ser
ENST00000520903.1:n.303G>A (RNF19A)
ENST00000523255.5:n.725G>A (RNF19A)
ENST00000616528.1:c.1942G>A (RNF19A)	ENSP00000480369.1:p.Gly648Ser
XM_005250853.2:c.1942G>A (RNF19A)	XP_005250910.1:p.Gly648Ser
XM_011516956.1:c.1780G>A (RNF19A)	XP_011515258.1:p.Gly594Ser
XM_011516956.3:c.1780G>A (RNF19A)	XP_011515258.1:p.Gly594Ser
XM_017013302.1:c.1942G>A (RNF19A)	XP_016868791.1:p.Gly648Ser
XM_017013303.2:c.1942G>A (RNF19A)	XP_016868792.1:p.Gly648Ser
XM_017013304.1:c.1780G>A (RNF19A)	XP_016868793.1:p.Gly594Ser
XM_024447118.1:c.1942G>A (RNF19A)	XP_024302886.1:p.Gly648Ser
XM_024447119.1:c.1942G>A (RNF19A)	XP_024302887.1:p.Gly648Ser
XM_024447120.1:c.1012G>A (RNF19A)	XP_024302888.1:p.Gly338Ser
XR_928315.1:n.2106G>A (RNF19A)
XR_928315.3:n.2051G>A (RNF19A)
XR_928316.1:n.1944G>A (RNF19A)