Canonical Allele Identifier: CA1979444880
Gene: EFEMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65868601G= , CM000673.2:g.65868601G= GRCh38
NC_000011.9:g.65636072G= , CM000673.1:g.65636072G= GRCh37
NC_000011.8:g.65392648G= NCBI36
NG_012304.2:g.9334C=
NG_053116.1:g.13540G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.756C= MANE Select ENSP00000309953.6:p.Tyr252=
ENST00000307998.10:c.756C= ENSP00000309953.6:p.Tyr252=
ENST00000526628.5:n.1322C=
ENST00000527969.1:n.1441C=
ENST00000528176.5:c.756C= ENSP00000434151.1:p.Tyr252=
ENST00000531005.5:n.1750C=
ENST00000531972.5:c.756C= ENSP00000435295.1:p.Tyr252=
ENST00000532084.5:n.182C=
NM_016938.4:c.756C= NP_058634.4:p.Tyr252=
NR_037718.1:n.1015C=
NM_016938.5:c.756C= MANE Select NP_058634.4:p.Tyr252=
NR_037718.2:n.881C=