Canonical Allele Identifier: CA1955396673

Gene: SERGEF

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18001867C>G , CM000673.2:g.18001867C>G	GRCh38
NC_000011.9:g.18023414C>G , CM000673.1:g.18023414C>G	GRCh37
NC_000011.8:g.17979990C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_012139.4:c.448-1310G>C MANE Select	NP_036271.1:n.448-1310G>C
ENST00000265965.10:c.448-1310G>C MANE Select	ENSP00000265965.5:n.448-1310G>C
NM_012139.3:c.448-1310G>C	NP_036271.1:n.448-1310G>C
NR_104040.1:n.600-1310G>C
NR_104040.2:n.485-1310G>C
NR_104041.1:n.600-1310G>C
NR_104041.2:n.485-1310G>C
ENST00000265965.9:c.448-1310G>C	ENSP00000265965.5:n.448-1310G>C
ENST00000524716.5:c.*390-1310G>C	ENSP00000433884.1:n.*390-1310G>C
ENST00000525422.5:c.448-1310G>C	ENSP00000434330.1:n.448-1310G>C
ENST00000525920.5:c.58-1310G>C	ENSP00000436648.1:n.58-1310G>C
ENST00000527494.5:c.106-1310G>C	ENSP00000431490.1:n.106-1310G>C
ENST00000528200.5:c.448-1310G>C	ENSP00000434188.1:n.448-1310G>C
ENST00000529728.5:c.106-1310G>C	ENSP00000437297.1:n.106-1310G>C
ENST00000530613.5:c.106-1310G>C	ENSP00000436080.1:n.106-1310G>C
ENST00000530925.5:c.*2+79G>C	ENSP00000433870.1:n.*2+79G>C
ENST00000532212.5:n.535-1310G>C
ENST00000532265.5:c.106-1310G>C	ENSP00000431314.1:n.106-1310G>C
ENST00000532389.5:c.106-1310G>C	ENSP00000435898.1:n.106-1310G>C
ENST00000533328.5:c.361-1310G>C	ENSP00000433383.1:n.361-1310G>C