Canonical Allele Identifier: CA2676683908

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177097453-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177097453T>C , CM000667.2:g.177097453T>C	GRCh38
NC_000005.9:g.176524454T>C , CM000667.1:g.176524454T>C	GRCh37
NC_000005.8:g.176457060T>C	NCBI36
NG_012067.1:g.15534T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000292408.9:c.2259+56T>C MANE Select	ENSP00000292408.4:n.2259+56T>C
ENST00000292408.8:c.2259+56T>C	ENSP00000292408.4:n.2259+56T>C
ENST00000393637.5:c.2139+56T>C	ENSP00000377254.1:n.2139+56T>C
ENST00000393648.6:c.2055+56T>C	ENSP00000377259.2:n.2055+56T>C
ENST00000502906.5:c.2259+56T>C	ENSP00000424960.1:n.2259+56T>C
ENST00000513423.1:n.207+56T>C
NM_001291980.1:c.2055+56T>C	NP_001278909.1:n.2055+56T>C
NM_002011.4:c.2259+56T>C	NP_002002.3:n.2259+56T>C
NM_022963.3:c.2139+56T>C	NP_075252.2:n.2139+56T>C
NM_213647.2:c.2259+56T>C	NP_998812.1:n.2259+56T>C
XM_005265838.2:c.2259+56T>C	XP_005265895.1:n.2259+56T>C
XM_011534464.1:c.2352+56T>C	XP_011532766.1:n.2352+56T>C
XM_011534465.1:c.1941+56T>C	XP_011532767.1:n.1941+56T>C
NM_001354984.1:c.2259+56T>C	NP_001341913.1:n.2259+56T>C
NM_213647.3:c.2259+56T>C MANE Select	NP_998812.1:n.2259+56T>C
NM_001291980.2:c.2055+56T>C	NP_001278909.1:n.2055+56T>C
NM_001354984.2:c.2259+56T>C	NP_001341913.1:n.2259+56T>C
NM_002011.5:c.2259+56T>C	NP_002002.3:n.2259+56T>C