Canonical Allele Identifier: CA561961121

Gene: FER

Linked Data

• dbSNP Id: rs1269804159
• gnomAD v2: 5-108113292-C-G
• gnomAD v3: 5-108777591-C-G
• gnomAD v4: 5-108777591-C-G
• MyVariant Identifiers: chr5:g.108113292C>G (hg19) ; chr5:g.108777591C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.108777591C>G , CM000667.2:g.108777591C>G	GRCh38
NC_000005.9:g.108113292C>G , CM000667.1:g.108113292C>G	GRCh37
NC_000005.8:g.108141191C>G	NCBI36
NG_011445.2:g.34770C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000281092.9:c.-60+9353C>G MANE Select	ENSP00000281092.4:n.-60+9353C>G
ENST00000281092.8:c.-60+9353C>G	ENSP00000281092.4:n.-60+9353C>G
ENST00000502752.1:n.174-5072C>G
ENST00000504143.6:c.-60+9353C>G	ENSP00000421951.2:n.-60+9353C>G
ENST00000509035.5:n.161-20533C>G
ENST00000513676.5:n.236-20533C>G
NM_001308028.1:c.-311+9353C>G	NP_001294957.1:n.-311+9353C>G
NM_001308038.1:c.-152-5072C>G	NP_001294967.1:n.-152-5072C>G
NM_005246.2:c.-60+9353C>G	NP_005237.2:n.-60+9353C>G
NM_005246.3:c.-60+9353C>G	NP_005237.2:n.-60+9353C>G
XM_011543266.1:c.-60+9353C>G	XP_011541568.1:n.-60+9353C>G
XM_011543267.1:c.-60+9353C>G	XP_011541569.1:n.-60+9353C>G
XM_011543268.1:c.-60+9353C>G	XP_011541570.1:n.-60+9353C>G
XM_011543269.1:c.-59-20533C>G	XP_011541571.1:n.-59-20533C>G
XM_011543270.1:c.-59-20533C>G	XP_011541572.1:n.-59-20533C>G
XM_011543271.1:c.-60+9353C>G	XP_011541573.1:n.-60+9353C>G
XM_011543272.1:c.-60+9353C>G	XP_011541574.1:n.-60+9353C>G
XM_011543275.1:c.-60+9353C>G	XP_011541577.1:n.-60+9353C>G
XM_011543278.1:c.-60+9353C>G	XP_011541580.1:n.-60+9353C>G
XR_948244.1:n.178+9353C>G
XR_948245.1:n.178+9353C>G
NR_146155.1:n.68-20533C>G
XM_011543266.2:c.-60+9353C>G	XP_011541568.1:n.-60+9353C>G
XM_011543267.2:c.-60+9353C>G	XP_011541569.1:n.-60+9353C>G
XM_011543269.2:c.-59-20533C>G	XP_011541571.1:n.-59-20533C>G
XM_011543270.3:c.-59-20533C>G	XP_011541572.1:n.-59-20533C>G
XM_011543271.3:c.-60+9353C>G	XP_011541573.1:n.-60+9353C>G
XM_011543272.2:c.-60+9353C>G	XP_011541574.1:n.-60+9353C>G
XM_017009229.2:c.-152-5072C>G	XP_016864718.1:n.-152-5072C>G
XM_017009230.2:c.-59-20533C>G	XP_016864719.1:n.-59-20533C>G
XM_017009231.2:c.-59-20533C>G	XP_016864720.1:n.-59-20533C>G
XM_017009232.2:c.15+9353C>G	XP_016864721.1:n.15+9353C>G
XM_017009234.1:c.-60+9353C>G	XP_016864723.1:n.-60+9353C>G
XM_017009235.1:c.-60+9353C>G	XP_016864724.1:n.-60+9353C>G
XR_001742041.1:n.178+9353C>G
XR_002956153.1:n.178+9353C>G
XR_948244.2:n.178+9353C>G
NM_005246.4:c.-60+9353C>G MANE Select	NP_005237.2:n.-60+9353C>G
NM_001308028.2:c.-311+9353C>G	NP_001294957.1:n.-311+9353C>G
NM_001308038.2:c.-152-5072C>G	NP_001294967.1:n.-152-5072C>G
NR_146155.2:n.47-20533C>G