Canonical Allele Identifier: CA1979444953
Gene: EFEMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65868632G= , CM000673.2:g.65868632G= GRCh38
NC_000011.9:g.65636103G= , CM000673.1:g.65636103G= GRCh37
NC_000011.8:g.65392679G= NCBI36
NG_012304.2:g.9303C=
NG_053116.1:g.13571G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.728-3C= MANE Select ENSP00000309953.6:n.728-3C=
ENST00000307998.10:c.728-3C= ENSP00000309953.6:n.728-3C=
ENST00000526628.5:n.1291C=
ENST00000527969.1:n.1410C=
ENST00000528176.5:c.728-3C= ENSP00000434151.1:n.728-3C=
ENST00000531005.5:n.1722-3C=
ENST00000531972.5:c.728-3C= ENSP00000435295.1:n.728-3C=
ENST00000532084.5:n.154-3C=
NM_016938.4:c.728-3C= NP_058634.4:n.728-3C=
NR_037718.1:n.987-3C=
NM_016938.5:c.728-3C= MANE Select NP_058634.4:n.728-3C=
NR_037718.2:n.853-3C=