Canonical Allele Identifier: CA206390948

Gene: MARCHF8

Linked Data

• dbSNP Id: rs1021945958
• gnomAD v4: 10-45459773-C-T
• MyVariant Identifiers: chr10:g.45955221C>T (hg19) ; chr10:g.45459773C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.45459773C>T , CM000672.2:g.45459773C>T	GRCh38
NC_000010.10:g.45955221C>T , CM000672.1:g.45955221C>T	GRCh37
NC_000010.9:g.45275227C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453424.7:c.1270-506G>A MANE Select	ENSP00000411848.2:n.1270-506G>A
ENST00000319836.7:c.424-506G>A	ENSP00000317087.3:n.424-506G>A
ENST00000395769.6:c.424-506G>A	ENSP00000379116.2:n.424-506G>A
ENST00000453424.6:c.1270-506G>A	ENSP00000411848.2:n.1270-506G>A
ENST00000476962.1:n.975-506G>A
NM_001002266.2:c.424-506G>A	NP_001002266.1:n.424-506G>A
NM_001282866.1:c.1270-506G>A	NP_001269795.1:n.1270-506G>A
NM_145021.5:c.424-506G>A	NP_659458.2:n.424-506G>A
XM_005271804.1:c.1270-506G>A	XP_005271861.1:n.1270-506G>A
XM_006717704.2:c.1270-506G>A	XP_006717767.1:n.1270-506G>A
XM_006717705.1:c.1270-506G>A	XP_006717768.1:n.1270-506G>A
XM_011539492.1:c.1270-506G>A	XP_011537794.1:n.1270-506G>A
XM_011539493.1:c.1270-506G>A	XP_011537795.1:n.1270-506G>A
XM_011539494.1:c.1270-506G>A	XP_011537796.1:n.1270-506G>A
XM_011539495.1:c.424-506G>A	XP_011537797.1:n.424-506G>A
XR_246519.1:n.2061G>A
XM_005271804.3:c.1270-506G>A	XP_005271861.1:n.1270-506G>A
XM_011539492.3:c.1270-506G>A	XP_011537794.1:n.1270-506G>A
XR_246519.3:n.2120G>A
NM_001282866.2:c.1270-506G>A MANE Select	NP_001269795.1:n.1270-506G>A
NM_001002266.3:c.424-506G>A	NP_001002266.1:n.424-506G>A
NM_145021.6:c.424-506G>A	NP_659458.2:n.424-506G>A
NM_001401645.1:c.1270-506G>A	NP_001388574.1:n.1270-506G>A
NM_001401646.1:c.1270-506G>A	NP_001388575.1:n.1270-506G>A