Canonical Allele Identifier: CA371650185
Gene: FZD6 HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.103300204A>C , CM000670.2:g.103300204A>C GRCh38
NC_000008.10:g.104312432A>C , CM000670.1:g.104312432A>C GRCh37
NC_000008.9:g.104381608A>C NCBI36
NG_028909.1:g.6772A>C
NG_028909.2:g.4211A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358755.5:c.97A>C MANE Select ENSP00000351605.4:p.Met33Leu
ENST00000358755.4:c.97A>C ENSP00000351605.4:p.Met33Leu
ENST00000519011.5:c.97A>C ENSP00000427733.1:p.Met33Leu
ENST00000521195.1:c.97A>C ENSP00000428188.1:p.Met33Leu
ENST00000522484.5:c.97A>C ENSP00000428301.1:p.Met33Leu
ENST00000522566.5:c.97A>C ENSP00000429055.1:p.Met33Leu
ENST00000523739.5:c.1A>C ENSP00000429528.1:p.Met1Leu
ENST00000523933.5:c.1A>C ENSP00000428257.1:p.Met1Leu
NM_001164615.1:c.97A>C NP_001158087.1:p.Met33Leu
NM_001164616.1:c.1A>C NP_001158088.1:p.Met1Leu
NM_003506.3:c.97A>C NP_003497.2:p.Met33Leu
XR_428385.2:n.347A>C
NM_001317796.1:c.-49A>C NP_001304725.1:n.-49A>C
NR_133921.1:n.414A>C
NM_003506.4:c.97A>C MANE Select NP_003497.2:p.Met33Leu
NM_001164615.2:c.97A>C NP_001158087.1:p.Met33Leu
NM_001164616.2:c.1A>C NP_001158088.1:p.Met1Leu
NM_001317796.2:c.-49A>C NP_001304725.1:n.-49A>C
NR_133921.2:n.414A>C