Canonical Allele Identifier: CA2684017596

Gene: MCM7 AP4M1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100101513A>T , CM000669.2:g.100101513A>T	GRCh38
NC_000007.13:g.99699136A>T , CM000669.1:g.99699136A>T	GRCh37
NC_000007.12:g.99537072A>T	NCBI36
NG_016312.1:g.5007A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001278595.1:c.-822T>A (MCM7)	NP_001265524.1:n.-822T>A
NM_004722.3:c.-202A>T (AP4M1)	NP_004713.2:n.-202A>T
NM_005916.4:c.-219T>A (MCM7)	NP_005907.3:n.-219T>A
ENST00000303887.9:c.-219T>A (MCM7)	ENSP00000307288.5:n.-219T>A
ENST00000343023.10:c.-219T>A (MCM7)	ENSP00000344006.6:n.-219T>A
ENST00000489841.6:n.428T>A (MCM7)
ENST00000621318.4:c.-822T>A (MCM7)	ENSP00000483795.1:n.-822T>A
ENST00000713591.1:c.-7-195A>T (AP4M1)	ENSP00000518888.1:n.-7-195A>T
XM_005250689.3:c.-8+17A>T (AP4M1)	XP_005250746.1:n.-8+17A>T
XM_005250689.4:c.-8+17A>T (AP4M1)	XP_005250746.1:n.-8+17A>T
XM_005250690.3:c.-202A>T (AP4M1)	XP_005250747.1:n.-202A>T
XM_005250690.4:c.-202A>T (AP4M1)	XP_005250747.1:n.-202A>T