Canonical Allele Identifier: CA10628120

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121598129C>G , CM000672.2:g.121598129C>G	GRCh38
NC_000010.10:g.123357643C>G , CM000672.1:g.123357643C>G	GRCh37
NC_000010.9:g.123347633C>G	NCBI36
NG_012449.1:g.5330G>C
NG_012449.2:g.5330G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.-318G>C MANE Plus Clinical	ENSP00000410294.2:n.-318G>C
ENST00000684153.1:c.-318G>C	ENSP00000506937.1:n.-318G>C
ENST00000358487.10:c.-318G>C MANE Select	ENSP00000351276.6:n.-318G>C
ENST00000336553.10:c.-318G>C	ENSP00000337665.6:n.-318G>C
ENST00000356226.8:c.-318G>C	ENSP00000348559.4:n.-318G>C
ENST00000359354.6:c.-318G>C	ENSP00000352309.2:n.-318G>C
ENST00000360144.7:c.-318G>C	ENSP00000353262.3:n.-318G>C
ENST00000369058.7:c.-318G>C	ENSP00000358054.3:n.-318G>C
ENST00000369059.5:c.-318G>C	ENSP00000358055.1:n.-318G>C
ENST00000369060.8:c.-318G>C	ENSP00000358056.4:n.-318G>C
ENST00000457416.6:c.-318G>C	ENSP00000410294.2:n.-318G>C
ENST00000604236.5:c.-318G>C	ENSP00000474109.1:n.-318G>C
ENST00000613048.4:c.-318G>C	ENSP00000484154.1:n.-318G>C
NM_000141.4:c.-318G>C	NP_000132.3:n.-318G>C
NM_001144917.1:c.-318G>C	NP_001138389.1:n.-318G>C
NM_001144918.1:c.-318G>C	NP_001138390.1:n.-318G>C
NM_001144919.1:c.-318G>C	NP_001138391.1:n.-318G>C
NM_022970.3:c.-318G>C	NP_075259.4:n.-318G>C
NR_073009.1:n.330G>C
XM_006717708.2:c.-261G>C	XP_006717771.1:n.-261G>C
XM_006717709.2:c.-261G>C	XP_006717772.1:n.-261G>C
XM_006717710.2:c.-261G>C	XP_006717773.1:n.-261G>C
XM_006717713.2:c.-261G>C	XP_006717776.1:n.-261G>C
NM_001320658.1:c.-318G>C	NP_001307587.1:n.-318G>C
XM_017015925.2:c.-261G>C	XP_016871414.1:n.-261G>C
XM_024447890.1:c.-261G>C	XP_024303658.1:n.-261G>C
NM_000141.5:c.-318G>C MANE Select	NP_000132.3:n.-318G>C
NM_001144917.2:c.-318G>C	NP_001138389.1:n.-318G>C
NM_001144918.2:c.-318G>C	NP_001138390.1:n.-318G>C
NM_001144919.2:c.-318G>C	NP_001138391.1:n.-318G>C
NM_001320658.2:c.-318G>C	NP_001307587.1:n.-318G>C
NR_073009.2:n.316G>C