Canonical Allele Identifier: CA1979444207
Gene: EFEMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65868437G= , CM000673.2:g.65868437G= GRCh38
NC_000011.9:g.65635908G= , CM000673.1:g.65635908G= GRCh37
NC_000011.8:g.65392484G= NCBI36
NG_012304.2:g.9498C=
NG_053116.1:g.13376G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.848-16C= MANE Select ENSP00000309953.6:n.848-16C=
ENST00000307998.10:c.848-16C= ENSP00000309953.6:n.848-16C=
ENST00000526628.5:n.1414-16C=
ENST00000528176.5:c.848-16C= ENSP00000434151.1:n.848-16C=
ENST00000528409.1:n.76C=
ENST00000530806.5:c.-151-16C= ENSP00000436526.1:n.-151-16C=
ENST00000531005.5:n.1842-16C=
ENST00000531972.5:c.848-16C= ENSP00000435295.1:n.848-16C=
ENST00000532084.5:n.274-16C=
NM_016938.4:c.848-16C= NP_058634.4:n.848-16C=
NR_037718.1:n.1107-16C=
NM_016938.5:c.848-16C= MANE Select NP_058634.4:n.848-16C=
NR_037718.2:n.973-16C=