Canonical Allele Identifier: CA2676681958

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177093104-T-TTGAC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093106_177093107insACTG , CM000667.2:g.177093106_177093107insACTG	GRCh38
NC_000005.9:g.176520107_176520108insACTG , CM000667.1:g.176520107_176520108insACTG	GRCh37
NC_000005.8:g.176452713_176452714insACTG	NCBI36
NG_012067.1:g.11187_11188insACTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1058-32_1058-31insACTG MANE Select	ENSP00000292408.4:n.1058-32_1058-31insACTG
ENST00000292408.8:c.1058-32_1058-31insACTG	ENSP00000292408.4:n.1058-32_1058-31insACTG
ENST00000393637.5:c.1058-226_1058-225insACTG	ENSP00000377254.1:n.1058-226_1058-225insACTG
ENST00000393648.6:c.1058-32_1058-31insACTG	ENSP00000377259.2:n.1058-32_1058-31insACTG
ENST00000502906.5:c.1058-32_1058-31insACTG	ENSP00000424960.1:n.1058-32_1058-31insACTG
ENST00000508139.1:n.362-32_362-31insACTG
NM_001291980.1:c.1058-32_1058-31insACTG	NP_001278909.1:n.1058-32_1058-31insACTG
NM_002011.4:c.1058-32_1058-31insACTG	NP_002002.3:n.1058-32_1058-31insACTG
NM_022963.3:c.1058-226_1058-225insACTG	NP_075252.2:n.1058-226_1058-225insACTG
NM_213647.2:c.1058-32_1058-31insACTG	NP_998812.1:n.1058-32_1058-31insACTG
XM_005265838.2:c.1058-32_1058-31insACTG	XP_005265895.1:n.1058-32_1058-31insACTG
XM_011534464.1:c.1151-32_1151-31insACTG	XP_011532766.1:n.1151-32_1151-31insACTG
XM_011534465.1:c.740-32_740-31insACTG	XP_011532767.1:n.740-32_740-31insACTG
XR_941090.1:n.1103-32_1103-31insACTG
NM_001354984.1:c.1058-32_1058-31insACTG	NP_001341913.1:n.1058-32_1058-31insACTG
NM_213647.3:c.1058-32_1058-31insACTG MANE Select	NP_998812.1:n.1058-32_1058-31insACTG
NM_001291980.2:c.1058-32_1058-31insACTG	NP_001278909.1:n.1058-32_1058-31insACTG
NM_001354984.2:c.1058-32_1058-31insACTG	NP_001341913.1:n.1058-32_1058-31insACTG
NM_002011.5:c.1058-32_1058-31insACTG	NP_002002.3:n.1058-32_1058-31insACTG