Canonical Allele Identifier: CA2643530207

Gene: FBLIM1

Linked Data

• gnomAD v4: 1-15768486-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15768486C>T , CM000663.2:g.15768486C>T	GRCh38
NC_000001.10:g.16094981C>T , CM000663.1:g.16094981C>T	GRCh37
NC_000001.9:g.15967568C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375766.8:c.439-42C>T MANE Select	ENSP00000364921.3:n.439-42C>T
ENST00000332305.5:c.251-1923C>T	ENSP00000364920.2:n.251-1923C>T
ENST00000375766.7:c.439-42C>T	ENSP00000364921.3:n.439-42C>T
ENST00000375771.5:c.439-42C>T	ENSP00000364926.1:n.439-42C>T
ENST00000441801.6:c.439-42C>T	ENSP00000416387.2:n.439-42C>T
ENST00000502739.5:c.251-1923C>T	ENSP00000424920.1:n.251-1923C>T
NM_001024215.1:c.439-42C>T	NP_001019386.1:n.439-42C>T
NM_001024216.1:c.251-1923C>T	NP_001019387.1:n.251-1923C>T
NM_017556.2:c.439-42C>T	NP_060026.2:n.439-42C>T
XM_005245900.1:c.439-42C>T	XP_005245957.1:n.439-42C>T
XM_005245901.1:c.439-42C>T	XP_005245958.1:n.439-42C>T
XM_005245902.1:c.439-42C>T	XP_005245959.1:n.439-42C>T
XM_005245903.1:c.439-42C>T	XP_005245960.1:n.439-42C>T
XM_005245909.2:c.439-42C>T	XP_005245966.1:n.439-42C>T
XM_006710704.2:c.439-42C>T	XP_006710767.1:n.439-42C>T
XM_006710705.1:c.439-42C>T	XP_006710768.1:n.439-42C>T
XM_011541616.1:c.439-42C>T	XP_011539918.1:n.439-42C>T
XM_011541617.1:c.439-42C>T	XP_011539919.1:n.439-42C>T
XM_011541618.1:c.439-42C>T	XP_011539920.1:n.439-42C>T
XM_011541619.1:c.251-1923C>T	XP_011539921.1:n.251-1923C>T
XR_946670.1:n.949-42C>T
NM_001024216.2:c.251-1923C>T	NP_001019387.1:n.251-1923C>T
NM_001350151.1:c.439-42C>T	NP_001337080.1:n.439-42C>T
NM_017556.3:c.439-42C>T	NP_060026.2:n.439-42C>T
XM_006710704.3:c.439-42C>T	XP_006710767.1:n.439-42C>T
XM_011541616.2:c.439-42C>T	XP_011539918.1:n.439-42C>T
XM_011541617.2:c.439-42C>T	XP_011539919.1:n.439-42C>T
XM_011541618.3:c.439-42C>T	XP_011539920.1:n.439-42C>T
XM_017001519.2:c.439-42C>T	XP_016857008.1:n.439-42C>T
XM_017001520.2:c.439-42C>T	XP_016857009.1:n.439-42C>T
XM_017001521.2:c.439-42C>T	XP_016857010.1:n.439-42C>T
XM_017001523.1:c.439-42C>T	XP_016857012.1:n.439-42C>T
XM_017001524.1:c.439-42C>T	XP_016857013.1:n.439-42C>T
XM_017001525.1:c.439-42C>T	XP_016857014.1:n.439-42C>T
XM_017001526.2:c.439-42C>T	XP_016857015.1:n.439-42C>T
XM_024447751.1:c.439-42C>T	XP_024303519.1:n.439-42C>T
NM_017556.4:c.439-42C>T MANE Select	NP_060026.2:n.439-42C>T
NM_001024216.3:c.251-1923C>T	NP_001019387.1:n.251-1923C>T
NM_001350151.2:c.439-42C>T	NP_001337080.1:n.439-42C>T