Canonical Allele Identifier: CA6322191
Community Standard Title: NM_002855.5(NECTIN1):c.79+4A>G
Gene: NECTIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119728471T>C , CM000673.2:g.119728471T>C GRCh38
NC_000011.9:g.119599181T>C , CM000673.1:g.119599181T>C GRCh37
NC_000011.8:g.119104391T>C NCBI36
NG_013083.1:g.5255A>G
NG_013083.2:g.5255A>G

Transcript Alleles

HGVS Amino-acid Change
NM_002855.5:c.79+4A>G MANE Select NP_002846.3:n.79+4A>G
ENST00000264025.8:c.79+4A>G MANE Select ENSP00000264025.3:n.79+4A>G
NM_002855.4:c.79+4A>G NP_002846.3:n.79+4A>G
NM_203285.1:c.79+4A>G NP_976030.1:n.79+4A>G
NM_203285.2:c.79+4A>G NP_976030.1:n.79+4A>G
NM_203286.1:c.79+4A>G NP_976031.1:n.79+4A>G
NM_203286.2:c.79+4A>G NP_976031.1:n.79+4A>G
ENST00000264025.7:c.79+4A>G ENSP00000264025.3:n.79+4A>G
ENST00000340882.2:c.79+4A>G ENSP00000345289.2:n.79+4A>G
ENST00000341398.6:c.79+4A>G ENSP00000344974.2:n.79+4A>G
ENST00000531468.2:c.79+4A>G ENSP00000513010.1:n.79+4A>G