Canonical Allele Identifier: CA13869031

Gene: MCF2L

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113004794G>A , CM000675.2:g.113004794G>A	GRCh38
NC_000013.10:g.113659108G>A , CM000675.1:g.113659108G>A	GRCh37
NC_000013.9:g.112707109G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420013.6:c.53-9969G>A	ENSP00000404422.2:n.53-9969G>A
ENST00000453297.6:c.80-9969G>A	ENSP00000392953.2:n.80-9969G>A
ENST00000704386.1:c.53-9969G>A	ENSP00000515888.1:n.53-9969G>A
ENST00000535094.7:c.80-9969G>A MANE Select	ENSP00000440374.2:n.80-9969G>A
ENST00000375597.8:c.73+2811G>A	ENSP00000364747.4:n.73+2811G>A
ENST00000375604.6:c.73+2811G>A	ENSP00000364754.3:n.73+2811G>A
ENST00000375608.7:c.170-9969G>A	ENSP00000364758.3:n.170-9969G>A
ENST00000397024.1:c.73+2811G>A	ENSP00000380219.1:n.73+2811G>A
ENST00000397030.5:c.179-9969G>A	ENSP00000380225.1:n.179-9969G>A
ENST00000409954.6:c.-9+3369G>A	ENSP00000386551.2:n.-9+3369G>A
ENST00000421756.5:c.92-9969G>A	ENSP00000397285.1:n.92-9969G>A
ENST00000433807.5:c.98-9969G>A	ENSP00000395707.1:n.98-9969G>A
ENST00000486210.1:n.199+2811G>A
ENST00000535094.6:c.80-9969G>A	ENSP00000440374.2:n.80-9969G>A
NM_001112732.2:c.80-9969G>A	NP_001106203.2:n.80-9969G>A
NM_024979.4:c.73+2811G>A	NP_079255.4:n.73+2811G>A
XM_005268309.2:c.170-9969G>A	XP_005268366.1:n.170-9969G>A
XM_005268314.2:c.92-9969G>A	XP_005268371.1:n.92-9969G>A
XM_005268316.1:c.73+2811G>A	XP_005268373.1:n.73+2811G>A
XM_011537482.1:c.170-9969G>A	XP_011535784.1:n.170-9969G>A
XM_011537483.1:c.170-9969G>A	XP_011535785.1:n.170-9969G>A
XM_011537484.1:c.92-9969G>A	XP_011535786.1:n.92-9969G>A
XM_011537485.1:c.80-9969G>A	XP_011535787.1:n.80-9969G>A
XM_011537486.1:c.77-9969G>A	XP_011535788.1:n.77-9969G>A
XM_011537487.1:c.73+2811G>A	XP_011535789.1:n.73+2811G>A
XM_011537488.1:c.26-9969G>A	XP_011535790.1:n.26-9969G>A
XM_011537489.1:c.170-9969G>A	XP_011535791.1:n.170-9969G>A
XM_011537490.1:c.-8-9969G>A	XP_011535792.1:n.-8-9969G>A
XM_011537492.1:c.170-9969G>A	XP_011535794.1:n.170-9969G>A
XM_011537493.1:c.77-9969G>A	XP_011535795.1:n.77-9969G>A
NM_001320815.1:c.73+2811G>A	NP_001307744.1:n.73+2811G>A
NM_001320816.1:c.92-9969G>A	NP_001307745.1:n.92-9969G>A
NM_001320817.1:c.73+2811G>A	NP_001307746.1:n.73+2811G>A
NM_001366644.1:c.-8-9969G>A	NP_001353573.1:n.-8-9969G>A
XM_011537483.2:c.170-9969G>A	XP_011535785.1:n.170-9969G>A
XM_011537486.2:c.251-9969G>A	XP_011535788.2:n.251-9969G>A
XM_017020493.1:c.251-9969G>A	XP_016875982.1:n.251-9969G>A
XM_017020494.1:c.98-9969G>A	XP_016875983.1:n.98-9969G>A
XM_017020495.1:c.251-9969G>A	XP_016875984.1:n.251-9969G>A
XM_017020499.2:c.251-9969G>A	XP_016875988.1:n.251-9969G>A
XR_001750037.1:n.1696G>A
NM_001112732.3:c.80-9969G>A MANE Select	NP_001106203.2:n.80-9969G>A
NM_001320815.2:c.73+2811G>A	NP_001307744.1:n.73+2811G>A
NM_001320816.2:c.92-9969G>A	NP_001307745.1:n.92-9969G>A
NM_001320817.2:c.73+2811G>A	NP_001307746.1:n.73+2811G>A
NM_001366644.2:c.-8-9969G>A	NP_001353573.1:n.-8-9969G>A