Canonical Allele Identifier: CA383282138
Gene: NECTIN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119677776G>C , CM000673.2:g.119677776G>C GRCh38
NC_000011.9:g.119548486G>C , CM000673.1:g.119548486G>C GRCh37
NC_000011.8:g.119053696G>C NCBI36
NG_013083.1:g.55950C>G
NG_013083.2:g.55950C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000531468.2:c.512C>G ENSP00000513010.1:p.Thr171Ser
ENST00000264025.8:c.512C>G MANE Select ENSP00000264025.3:p.Thr171Ser
ENST00000264025.7:c.512C>G ENSP00000264025.3:p.Thr171Ser
ENST00000340882.2:c.512C>G ENSP00000345289.2:p.Thr171Ser
ENST00000341398.6:c.512C>G ENSP00000344974.2:p.Thr171Ser
ENST00000524510.1:n.486C>G
NM_002855.4:c.512C>G NP_002846.3:p.Thr171Ser
NM_203285.1:c.512C>G NP_976030.1:p.Thr171Ser
NM_203286.1:c.512C>G NP_976031.1:p.Thr171Ser
NM_002855.5:c.512C>G MANE Select NP_002846.3:p.Thr171Ser
NM_203285.2:c.512C>G NP_976030.1:p.Thr171Ser
NM_203286.2:c.512C>G NP_976031.1:p.Thr171Ser