Canonical Allele Identifier: CA4742443

Gene: MCM4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.47966173T>C , CM000670.2:g.47966173T>C	GRCh38
NC_000008.10:g.48878733T>C , CM000670.1:g.48878733T>C	GRCh37
NC_000008.9:g.49041286T>C	NCBI36
NG_032967.1:g.10971T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697120.1:n.928-14T>C
ENST00000697121.1:n.1006-14T>C
ENST00000697122.1:c.833-14T>C	ENSP00000513122.1:n.833-14T>C
ENST00000520637.2:c.122-14T>C	ENSP00000427875.2:n.122-14T>C
ENST00000647877.1:c.247-1192T>C
ENST00000648407.1:c.833-14T>C	ENSP00000497881.1:n.833-14T>C
ENST00000648519.1:c.*562-14T>C	ENSP00000497176.1:n.*562-14T>C
ENST00000649838.1:c.833-14T>C	ENSP00000497648.1:n.833-14T>C
ENST00000649919.1:c.683-14T>C	ENSP00000498202.1:n.683-14T>C
ENST00000649973.1:c.833-14T>C MANE Select	ENSP00000496964.1:n.833-14T>C
ENST00000650216.1:c.832+1461T>C	ENSP00000497093.1:n.832+1461T>C
ENST00000262105.6:c.833-14T>C	ENSP00000262105.2:n.833-14T>C
ENST00000519138.1:n.794-14T>C
ENST00000520637.1:c.119-14T>C	ENSP00000427875.1:n.119-14T>C
ENST00000523944.5:c.833-14T>C	ENSP00000430194.1:n.833-14T>C
NM_005914.3:c.833-14T>C	NP_005905.2:n.833-14T>C
NM_182746.2:c.833-14T>C	NP_877423.1:n.833-14T>C
XM_005251234.1:c.683-14T>C	XP_005251291.1:n.683-14T>C
NM_005914.4:c.833-14T>C	NP_005905.2:n.833-14T>C
NM_182746.3:c.833-14T>C MANE Select	NP_877423.1:n.833-14T>C