Canonical Allele Identifier: CA1137501701
Gene: GPC3 HGNC NCBI

Linked Data

dbSNP Id: rs2076399511

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.133952956T>C , CM000685.2:g.133952956T>C GRCh38
NC_000023.10:g.133086983T>C , CM000685.1:g.133086983T>C GRCh37
NC_000023.9:g.132914649T>C NCBI36
NG_009286.1:g.37684A>G , LRG_505:g.37684A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000684880.1:c.337+94A>G ENSP00000510280.1:n.337+94A>G
ENST00000689310.1:c.289+142A>G ENSP00000510438.1:n.289+142A>G
ENST00000692630.1:n.467+94A>G
ENST00000370818.8:c.337+94A>G MANE Select ENSP00000359854.3:n.337+94A>G
ENST00000394299.7:c.337+94A>G ENSP00000377836.2:n.337+94A>G
ENST00000370818.7:c.337+94A>G ENSP00000359854.3:n.337+94A>G
ENST00000394299.6:c.337+94A>G ENSP00000377836.2:n.337+94A>G
ENST00000631057.2:c.175+32319A>G ENSP00000486325.1:n.175+32319A>G
NM_001164617.1:c.337+94A>G NP_001158089.1:n.337+94A>G
NM_001164618.1:c.289+142A>G NP_001158090.1:n.289+142A>G
NM_001164619.1:c.175+32319A>G NP_001158091.1:n.175+32319A>G
NM_004484.3:c.337+94A>G , LRG_505t1:c.337+94A>G NP_004475.1:n.337+94A>G
XM_017029413.2:c.337+94A>G XP_016884902.1:n.337+94A>G
NM_001164617.2:c.337+94A>G NP_001158089.1:n.337+94A>G
NM_001164618.2:c.289+142A>G NP_001158090.1:n.289+142A>G
NM_001164619.2:c.175+32319A>G NP_001158091.1:n.175+32319A>G
NM_004484.4:c.337+94A>G MANE Select NP_004475.1:n.337+94A>G