Canonical Allele Identifier: CA2676682297

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177093567-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177093567_177093568insA , CM000667.2:g.177093567_177093568insA	GRCh38
NC_000005.9:g.176520568_176520569insA , CM000667.1:g.176520568_176520569insA	GRCh37
NC_000005.8:g.176453174_176453175insA	NCBI36
NG_012067.1:g.11648_11649insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.1397+16_1397+17insA MANE Select	ENSP00000292408.4:n.1397+16_1397+17insA
ENST00000292408.8:c.1397+16_1397+17insA	ENSP00000292408.4:n.1397+16_1397+17insA
ENST00000393637.5:c.1277+16_1277+17insA	ENSP00000377254.1:n.1277+16_1277+17insA
ENST00000393648.6:c.1193+66_1193+67insA	ENSP00000377259.2:n.1193+66_1193+67insA
ENST00000502906.5:c.1397+16_1397+17insA	ENSP00000424960.1:n.1397+16_1397+17insA
ENST00000511076.1:c.291+16_291+17insA
NM_001291980.1:c.1193+66_1193+67insA	NP_001278909.1:n.1193+66_1193+67insA
NM_002011.4:c.1397+16_1397+17insA	NP_002002.3:n.1397+16_1397+17insA
NM_022963.3:c.1277+16_1277+17insA	NP_075252.2:n.1277+16_1277+17insA
NM_213647.2:c.1397+16_1397+17insA	NP_998812.1:n.1397+16_1397+17insA
XM_005265838.2:c.1397+16_1397+17insA	XP_005265895.1:n.1397+16_1397+17insA
XM_011534464.1:c.1490+16_1490+17insA	XP_011532766.1:n.1490+16_1490+17insA
XM_011534465.1:c.1079+16_1079+17insA	XP_011532767.1:n.1079+16_1079+17insA
XR_941090.1:n.1392+66_1392+67insA
NM_001354984.1:c.1397+16_1397+17insA	NP_001341913.1:n.1397+16_1397+17insA
NM_213647.3:c.1397+16_1397+17insA MANE Select	NP_998812.1:n.1397+16_1397+17insA
NM_001291980.2:c.1193+66_1193+67insA	NP_001278909.1:n.1193+66_1193+67insA
NM_001354984.2:c.1397+16_1397+17insA	NP_001341913.1:n.1397+16_1397+17insA
NM_002011.5:c.1397+16_1397+17insA	NP_002002.3:n.1397+16_1397+17insA