Canonical Allele Identifier: CA839890375
Gene: FSCN1 HGNC NCBI

Linked Data

dbSNP Id: rs1383733604
MyVariant Identifiers: chr7:g.5642807G>C (hg19) chr7:g.5603176G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5603176G>C , CM000669.2:g.5603176G>C GRCh38
NC_000007.13:g.5642807G>C , CM000669.1:g.5642807G>C GRCh37
NC_000007.12:g.5609333G>C NCBI36
NG_030004.1:g.15372G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382361.8:c.833-81G>C MANE Select ENSP00000371798.3:n.833-81G>C
ENST00000382361.7:c.833-81G>C ENSP00000371798.3:n.833-81G>C
ENST00000405801.2:c.-2-81G>C ENSP00000383982.2:n.-2-81G>C
ENST00000444748.5:c.-2-81G>C ENSP00000404506.1:n.-2-81G>C
ENST00000447103.5:c.-2-81G>C ENSP00000409967.1:n.-2-81G>C
ENST00000473330.1:n.305G>C
NM_003088.3:c.833-81G>C NP_003079.1:n.833-81G>C
NM_003088.4:c.833-81G>C MANE Select NP_003079.1:n.833-81G>C
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