Canonical Allele Identifier: CA1571393439

Gene: FER

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.108777690_108777694delinsAAAAG , CM000667.2:g.108777690_108777694delinsAAAAG	GRCh38
NC_000005.9:g.108113391_108113395delinsAAAAG , CM000667.1:g.108113391_108113395delinsAAAAG	GRCh37
NC_000005.8:g.108141290_108141294delinsAAAAG	NCBI36
NG_011445.2:g.34869_34873delinsAAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281092.9:c.-60+9452_-60+9456delinsAAAAG MANE Select	ENSP00000281092.4:n.-60+9452_-60+9456delinsAAAAG
ENST00000281092.8:c.-60+9452_-60+9456delinsAAAAG	ENSP00000281092.4:n.-60+9452_-60+9456delinsAAAAG
ENST00000502752.1:n.174-4973_174-4969delinsAAAAG
ENST00000504143.6:c.-60+9452_-60+9456delinsAAAAG	ENSP00000421951.2:n.-60+9452_-60+9456delinsAAAAG
ENST00000509035.5:n.161-20434_161-20430delinsAAAAG
ENST00000513676.5:n.236-20434_236-20430delinsAAAAG
NM_001308028.1:c.-311+9452_-311+9456delinsAAAAG	NP_001294957.1:n.-311+9452_-311+9456delinsAAAAG
NM_001308038.1:c.-152-4973_-152-4969delinsAAAAG	NP_001294967.1:n.-152-4973_-152-4969delinsAAAAG
NM_005246.2:c.-60+9452_-60+9456delinsAAAAG	NP_005237.2:n.-60+9452_-60+9456delinsAAAAG
NM_005246.3:c.-60+9452_-60+9456delinsAAAAG	NP_005237.2:n.-60+9452_-60+9456delinsAAAAG
XM_011543266.1:c.-60+9452_-60+9456delinsAAAAG	XP_011541568.1:n.-60+9452_-60+9456delinsAAAAG
XM_011543267.1:c.-60+9452_-60+9456delinsAAAAG	XP_011541569.1:n.-60+9452_-60+9456delinsAAAAG
XM_011543268.1:c.-60+9452_-60+9456delinsAAAAG	XP_011541570.1:n.-60+9452_-60+9456delinsAAAAG
XM_011543269.1:c.-59-20434_-59-20430delinsAAAAG	XP_011541571.1:n.-59-20434_-59-20430delinsAAAAG
XM_011543270.1:c.-59-20434_-59-20430delinsAAAAG	XP_011541572.1:n.-59-20434_-59-20430delinsAAAAG
XM_011543271.1:c.-60+9452_-60+9456delinsAAAAG	XP_011541573.1:n.-60+9452_-60+9456delinsAAAAG
XM_011543272.1:c.-60+9452_-60+9456delinsAAAAG	XP_011541574.1:n.-60+9452_-60+9456delinsAAAAG
XM_011543275.1:c.-60+9452_-60+9456delinsAAAAG	XP_011541577.1:n.-60+9452_-60+9456delinsAAAAG
XM_011543278.1:c.-60+9452_-60+9456delinsAAAAG	XP_011541580.1:n.-60+9452_-60+9456delinsAAAAG
XR_948244.1:n.178+9452_178+9456delinsAAAAG
XR_948245.1:n.178+9452_178+9456delinsAAAAG
NR_146155.1:n.68-20434_68-20430delinsAAAAG
XM_011543266.2:c.-60+9452_-60+9456delinsAAAAG	XP_011541568.1:n.-60+9452_-60+9456delinsAAAAG
XM_011543267.2:c.-60+9452_-60+9456delinsAAAAG	XP_011541569.1:n.-60+9452_-60+9456delinsAAAAG
XM_011543269.2:c.-59-20434_-59-20430delinsAAAAG	XP_011541571.1:n.-59-20434_-59-20430delinsAAAAG
XM_011543270.3:c.-59-20434_-59-20430delinsAAAAG	XP_011541572.1:n.-59-20434_-59-20430delinsAAAAG
XM_011543271.3:c.-60+9452_-60+9456delinsAAAAG	XP_011541573.1:n.-60+9452_-60+9456delinsAAAAG
XM_011543272.2:c.-60+9452_-60+9456delinsAAAAG	XP_011541574.1:n.-60+9452_-60+9456delinsAAAAG
XM_017009229.2:c.-152-4973_-152-4969delinsAAAAG	XP_016864718.1:n.-152-4973_-152-4969delinsAAAAG
XM_017009230.2:c.-59-20434_-59-20430delinsAAAAG	XP_016864719.1:n.-59-20434_-59-20430delinsAAAAG
XM_017009231.2:c.-59-20434_-59-20430delinsAAAAG	XP_016864720.1:n.-59-20434_-59-20430delinsAAAAG
XM_017009232.2:c.15+9452_15+9456delinsAAAAG	XP_016864721.1:n.15+9452_15+9456delinsAAAAG
XM_017009234.1:c.-60+9452_-60+9456delinsAAAAG	XP_016864723.1:n.-60+9452_-60+9456delinsAAAAG
XM_017009235.1:c.-60+9452_-60+9456delinsAAAAG	XP_016864724.1:n.-60+9452_-60+9456delinsAAAAG
XR_001742041.1:n.178+9452_178+9456delinsAAAAG
XR_002956153.1:n.178+9452_178+9456delinsAAAAG
XR_948244.2:n.178+9452_178+9456delinsAAAAG
NM_005246.4:c.-60+9452_-60+9456delinsAAAAG MANE Select	NP_005237.2:n.-60+9452_-60+9456delinsAAAAG
NM_001308028.2:c.-311+9452_-311+9456delinsAAAAG	NP_001294957.1:n.-311+9452_-311+9456delinsAAAAG
NM_001308038.2:c.-152-4973_-152-4969delinsAAAAG	NP_001294967.1:n.-152-4973_-152-4969delinsAAAAG
NR_146155.2:n.47-20434_47-20430delinsAAAAG