Canonical Allele Identifier: CA1139773489

Gene: MEAF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.37493212C= , CM000663.2:g.37493212C=	GRCh38
NC_000001.10:g.37958813C= , CM000663.1:g.37958813C=	GRCh37
NC_000001.9:g.37731400C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001270875.3:c.*887G= MANE Select	NP_001257804.1:n.*887G=
ENST00000296214.10:c.*887G= MANE Select	ENSP00000296214.5:n.*887G=
NM_001270875.1:c.*887G=	NP_001257804.1:n.*887G=
NM_001270875.2:c.*887G=	NP_001257804.1:n.*887G=
NM_001270876.1:c.*557G=	NP_001257805.1:n.*557G=
NM_001270876.2:c.*557G=	NP_001257805.1:n.*557G=
NM_001270876.3:c.*557G=	NP_001257805.1:n.*557G=
NM_022756.5:c.*887G=	NP_073593.2:n.*887G=
NM_022756.6:c.*887G=	NP_073593.2:n.*887G=
NM_022756.7:c.*887G=	NP_073593.2:n.*887G=
NR_073090.1:n.1624G=
NR_073090.2:n.1571G=
NR_073090.3:n.1571G=
NR_073091.1:n.1594G=
NR_073091.2:n.1541G=
NR_073091.3:n.1541G=
NR_073092.1:n.1655G=
NR_073092.2:n.1602G=
NR_073092.3:n.1602G=
ENST00000296214.9:c.*887G=	ENSP00000296214.5:n.*887G=
ENST00000373075.6:c.*887G=	ENSP00000362166.2:n.*887G=