Canonical Allele Identifier: CA214327357

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121598437G>T , CM000672.2:g.121598437G>T	GRCh38
NC_000010.10:g.123357951G>T , CM000672.1:g.123357951G>T	GRCh37
NC_000010.9:g.123347941G>T	NCBI36
NG_012449.1:g.5022C>A
NG_012449.2:g.5022C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.-626C>A MANE Plus Clinical	ENSP00000410294.2:n.-626C>A
ENST00000358487.10:c.-626C>A MANE Select	ENSP00000351276.6:n.-626C>A
ENST00000356226.8:c.-626C>A	ENSP00000348559.4:n.-626C>A
ENST00000369059.5:c.-626C>A	ENSP00000358055.1:n.-626C>A
ENST00000613048.4:c.-626C>A	ENSP00000484154.1:n.-626C>A
NM_000141.4:c.-626C>A	NP_000132.3:n.-626C>A
NM_001144917.1:c.-626C>A	NP_001138389.1:n.-626C>A
NM_001144918.1:c.-626C>A	NP_001138390.1:n.-626C>A
NM_001144919.1:c.-626C>A	NP_001138391.1:n.-626C>A
NM_022970.3:c.-626C>A	NP_075259.4:n.-626C>A
NR_073009.1:n.22C>A
XM_006717708.2:c.-569C>A	XP_006717771.1:n.-569C>A
XM_006717709.2:c.-569C>A	XP_006717772.1:n.-569C>A
XM_006717710.2:c.-569C>A	XP_006717773.1:n.-569C>A
XM_006717713.2:c.-569C>A	XP_006717776.1:n.-569C>A
NM_001320658.1:c.-626C>A	NP_001307587.1:n.-626C>A
XM_024447890.1:c.-569C>A	XP_024303658.1:n.-569C>A
NM_000141.5:c.-626C>A MANE Select	NP_000132.3:n.-626C>A
NM_001144917.2:c.-626C>A	NP_001138389.1:n.-626C>A
NM_001144918.2:c.-626C>A	NP_001138390.1:n.-626C>A
NM_001144919.2:c.-626C>A	NP_001138391.1:n.-626C>A
NM_001320658.2:c.-626C>A	NP_001307587.1:n.-626C>A
NR_073009.2:n.8C>A