Canonical Allele Identifier: CA343055131
Community Standard Title: NM_001127173.3(CADM3):c.413A>G (p.Tyr138Cys)
Gene: CADM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159193453A>G , CM000663.2:g.159193453A>G GRCh38
NC_000001.10:g.159163243A>G , CM000663.1:g.159163243A>G GRCh37
NC_000001.9:g.157429867A>G NCBI36
NG_051933.1:g.26890A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001127173.3:c.413A>G MANE Select NP_001120645.1:p.Tyr138Cys
ENST00000368125.9:c.413A>G MANE Select ENSP00000357107.4:p.Tyr138Cys
NM_001127173.1:c.413A>G NP_001120645.1:p.Tyr138Cys
NM_001127173.2:c.413A>G NP_001120645.1:p.Tyr138Cys
NM_001346510.1:c.413A>G NP_001333439.1:p.Tyr138Cys
NM_001346510.2:c.413A>G NP_001333439.1:p.Tyr138Cys
NM_021189.3:c.515A>G NP_067012.1:p.Tyr172Cys
NM_021189.4:c.515A>G NP_067012.1:p.Tyr172Cys
NM_021189.5:c.515A>G NP_067012.1:p.Tyr172Cys
ENST00000368124.8:c.515A>G ENSP00000357106.4:p.Tyr172Cys
ENST00000368125.8:c.413A>G ENSP00000357107.4:p.Tyr138Cys
ENST00000416746.1:c.413A>G ENSP00000387802.1:p.Tyr138Cys
XM_024448760.1:c.662A>G XP_024304528.1:p.Tyr221Cys