Canonical Allele Identifier: CA2838197238

Gene: CADM3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159192810G>T , CM000663.2:g.159192810G>T	GRCh38
NC_000001.10:g.159162600G>T , CM000663.1:g.159162600G>T	GRCh37
NC_000001.9:g.157429224G>T	NCBI36
NG_051933.1:g.26247G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368125.9:c.382+80G>T MANE Select	ENSP00000357107.4:n.382+80G>T
ENST00000368124.8:c.484+80G>T	ENSP00000357106.4:n.484+80G>T
ENST00000368125.8:c.382+80G>T	ENSP00000357107.4:n.382+80G>T
ENST00000416746.1:c.382+80G>T	ENSP00000387802.1:n.382+80G>T
NM_001127173.1:c.382+80G>T	NP_001120645.1:n.382+80G>T
NM_021189.3:c.484+80G>T	NP_067012.1:n.484+80G>T
NM_001127173.2:c.382+80G>T	NP_001120645.1:n.382+80G>T
NM_001346510.1:c.382+80G>T	NP_001333439.1:n.382+80G>T
NM_021189.4:c.484+80G>T	NP_067012.1:n.484+80G>T
XM_024448760.1:c.631+80G>T	XP_024304528.1:n.631+80G>T
NM_001127173.3:c.382+80G>T MANE Select	NP_001120645.1:n.382+80G>T
NM_001346510.2:c.382+80G>T	NP_001333439.1:n.382+80G>T
NM_021189.5:c.484+80G>T	NP_067012.1:n.484+80G>T