Canonical Allele Identifier: CA2676680986

Gene: FGFR4

Linked Data

• gnomAD v4: 5-177090796-C-CTGACCT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177090796_177090797insTGACCT , CM000667.2:g.177090796_177090797insTGACCT	GRCh38
NC_000005.9:g.176517797_176517798insTGACCT , CM000667.1:g.176517797_176517798insTGACCT	GRCh37
NC_000005.8:g.176450403_176450404insTGACCT	NCBI36
NG_012067.1:g.8877_8878insTGACCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292408.9:c.407_408insTGACCT MANE Select	ENSP00000292408.4:p.Pro136_Ser137insAspLeu
ENST00000292408.8:c.407_408insTGACCT	ENSP00000292408.4:p.Pro136_Ser137insAspLeu
ENST00000393637.5:c.407_408insTGACCT	ENSP00000377254.1:p.Pro136_Ser137insAspLeu
ENST00000393648.6:c.407_408insTGACCT	ENSP00000377259.2:p.Pro136_Ser137insAspLeu
ENST00000426612.5:n.412_413insTGACCT
ENST00000430285.5:c.*271_*272insTGACCT	ENSP00000395164.1:n.*271_*272insTGACCT
ENST00000502906.5:c.407_408insTGACCT	ENSP00000424960.1:p.Pro136_Ser137insAspLeu
ENST00000503708.5:c.407_408insTGACCT	ENSP00000424905.1:p.Pro136_Ser137insAspLeu
ENST00000509511.5:n.407_408insTGACCT
NM_001291980.1:c.407_408insTGACCT	NP_001278909.1:p.Pro136_Ser137insAspLeu
NM_002011.4:c.407_408insTGACCT	NP_002002.3:p.Pro136_Ser137insAspLeu
NM_022963.3:c.407_408insTGACCT	NP_075252.2:p.Pro136_Ser137insAspLeu
NM_213647.2:c.407_408insTGACCT	NP_998812.1:p.Pro136_Ser137insAspLeu
XM_005265838.2:c.407_408insTGACCT	XP_005265895.1:p.Pro136_Ser137insAspLeu
XM_011534464.1:c.500_501insTGACCT	XP_011532766.1:p.Pro167_Ser168insAspLeu
XM_011534465.1:c.89_90insTGACCT	XP_011532767.1:p.Pro30_Ser31insAspLeu
XR_941090.1:n.452_453insTGACCT
NM_001354984.1:c.407_408insTGACCT	NP_001341913.1:p.Pro136_Ser137insAspLeu
NM_213647.3:c.407_408insTGACCT MANE Select	NP_998812.1:p.Pro136_Ser137insAspLeu
NM_001291980.2:c.407_408insTGACCT	NP_001278909.1:p.Pro136_Ser137insAspLeu
NM_001354984.2:c.407_408insTGACCT	NP_001341913.1:p.Pro136_Ser137insAspLeu
NM_002011.5:c.407_408insTGACCT	NP_002002.3:p.Pro136_Ser137insAspLeu