Canonical Allele Identifier: CA2018007985

Gene: MCF2L

Linked Data

• dbSNP Id: rs10665

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113098517A>T , CM000675.2:g.113098517A>T	GRCh38
NC_000013.10:g.113752831A>T , CM000675.1:g.113752831A>T	GRCh37
NC_000013.9:g.112800832A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000420013.6:c.*1658A>T	ENSP00000404422.2:n.*1658A>T
ENST00000453297.6:c.5204A>T	ENSP00000392953.2:n.5204A>T
ENST00000704386.1:c.*2139A>T	ENSP00000515888.1:n.*2139A>T
ENST00000535094.7:c.*1658A>T MANE Select	ENSP00000440374.2:n.*1658A>T
ENST00000375604.6:c.*1658A>T	ENSP00000364754.3:n.*1658A>T
ENST00000397030.5:c.*2030A>T	ENSP00000380225.1:n.*2030A>T
ENST00000469415.1:n.2996A>T
ENST00000488765.1:n.3176A>T
NM_001112732.2:c.*1658A>T	NP_001106203.2:n.*1658A>T
NM_024979.4:c.*1658A>T	NP_079255.4:n.*1658A>T
XM_005268309.2:c.*1658A>T	XP_005268366.1:n.*1658A>T
XM_011537482.1:c.*1658A>T	XP_011535784.1:n.*1658A>T
XM_011537483.1:c.*1658A>T	XP_011535785.1:n.*1658A>T
XM_011537484.1:c.*1658A>T	XP_011535786.1:n.*1658A>T
XM_011537485.1:c.*1658A>T	XP_011535787.1:n.*1658A>T
XM_011537486.1:c.*1658A>T	XP_011535788.1:n.*1658A>T
XM_011537487.1:c.*1658A>T	XP_011535789.1:n.*1658A>T
XM_011537488.1:c.*1658A>T	XP_011535790.1:n.*1658A>T
XM_011537489.1:c.*1658A>T	XP_011535791.1:n.*1658A>T
XM_011537490.1:c.*1658A>T	XP_011535792.1:n.*1658A>T
XM_011537491.1:c.*1658A>T	XP_011535793.1:n.*1658A>T
NM_001320815.1:c.*1658A>T	NP_001307744.1:n.*1658A>T
NM_001320816.1:c.*1658A>T	NP_001307745.1:n.*1658A>T
NM_001366644.1:c.*1658A>T	NP_001353573.1:n.*1658A>T
NM_001366645.1:c.*1658A>T	NP_001353574.1:n.*1658A>T
NM_001366646.1:c.*1658A>T	NP_001353575.1:n.*1658A>T
XM_011537483.2:c.*1658A>T	XP_011535785.1:n.*1658A>T
XM_011537486.2:c.*1658A>T	XP_011535788.2:n.*1658A>T
XM_017020493.1:c.*1658A>T	XP_016875982.1:n.*1658A>T
XM_017020494.1:c.*1658A>T	XP_016875983.1:n.*1658A>T
XM_017020495.1:c.*1658A>T	XP_016875984.1:n.*1658A>T
NM_001112732.3:c.*1658A>T MANE Select	NP_001106203.2:n.*1658A>T
NM_001320815.2:c.*1658A>T	NP_001307744.1:n.*1658A>T
NM_001320816.2:c.*1658A>T	NP_001307745.1:n.*1658A>T
NM_001366644.2:c.*1658A>T	NP_001353573.1:n.*1658A>T
NM_001366645.2:c.*1658A>T	NP_001353574.1:n.*1658A>T
NM_001366646.2:c.*1658A>T	NP_001353575.1:n.*1658A>T