Canonical Allele Identifier: CA1979444245
Gene: EFEMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65868445A= , CM000673.2:g.65868445A= GRCh38
NC_000011.9:g.65635916A= , CM000673.1:g.65635916A= GRCh37
NC_000011.8:g.65392492A= NCBI36
NG_012304.2:g.9490T=
NG_053116.1:g.13384A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.848-24T= MANE Select ENSP00000309953.6:n.848-24T=
ENST00000307998.10:c.848-24T= ENSP00000309953.6:n.848-24T=
ENST00000526628.5:n.1414-24T=
ENST00000528176.5:c.848-24T= ENSP00000434151.1:n.848-24T=
ENST00000528409.1:n.68T=
ENST00000530806.5:c.-151-24T= ENSP00000436526.1:n.-151-24T=
ENST00000531005.5:n.1842-24T=
ENST00000531972.5:c.848-24T= ENSP00000435295.1:n.848-24T=
ENST00000532084.5:n.274-24T=
NM_016938.4:c.848-24T= NP_058634.4:n.848-24T=
NR_037718.1:n.1107-24T=
NM_016938.5:c.848-24T= MANE Select NP_058634.4:n.848-24T=
NR_037718.2:n.973-24T=