Canonical Allele Identifier: CA7687312

Gene: MORF4L1

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78891502G>C , CM000677.2:g.78891502G>C	GRCh38
NC_000015.9:g.79183844G>C , CM000677.1:g.79183844G>C	GRCh37
NC_000015.8:g.76970899G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426013.7:c.368G>C MANE Select	ENSP00000408880.2:p.Gly123Ala
ENST00000331268.9:c.485G>C	ENSP00000331310.5:p.Gly162Ala
ENST00000379535.8:c.443G>C	ENSP00000368850.4:p.Gly148Ala
ENST00000426013.6:c.368G>C	ENSP00000408880.2:p.Gly123Ala
ENST00000558502.5:c.104G>C	ENSP00000452808.1:p.Gly35Ala
ENST00000558522.5:n.871G>C
ENST00000558746.5:c.287G>C	ENSP00000453231.1:p.Gly96Ala
ENST00000558830.5:c.104G>C	ENSP00000453738.1:p.Gly35Ala
ENST00000558893.5:n.332G>C
ENST00000558923.5:n.392G>C
ENST00000559158.5:c.104G>C	ENSP00000453432.1:p.Gly35Ala
ENST00000559244.5:c.104G>C	ENSP00000454030.1:p.Gly35Ala
ENST00000559258.5:n.812G>C
ENST00000559345.5:c.104G>C	ENSP00000452717.1:p.Gly35Ala
ENST00000559690.5:c.104G>C	ENSP00000453351.1:p.Gly35Ala
ENST00000559751.1:c.415G>C
ENST00000559930.5:c.104G>C	ENSP00000454191.1:p.Gly35Ala
ENST00000560422.5:c.398G>C	ENSP00000453625.1:p.Gly133Ala
ENST00000561171.5:n.317-3318G>C
NM_001265603.1:c.104G>C	NP_001252532.1:p.Gly35Ala
NM_001265604.1:c.104G>C	NP_001252533.1:p.Gly35Ala
NM_001265605.1:c.104G>C	NP_001252534.1:p.Gly35Ala
NM_006791.3:c.368G>C	NP_006782.1:p.Gly123Ala
NM_206839.2:c.485G>C	NP_996670.1:p.Gly162Ala
NM_006791.4:c.368G>C MANE Select	NP_006782.1:p.Gly123Ala
NM_001265603.2:c.104G>C	NP_001252532.1:p.Gly35Ala
NM_001265604.2:c.104G>C	NP_001252533.1:p.Gly35Ala
NM_001265605.2:c.104G>C	NP_001252534.1:p.Gly35Ala
NM_206839.3:c.485G>C	NP_996670.1:p.Gly162Ala