Canonical Allele Identifier: CA381353136

Gene: EFEMP2

Linked Data

• MyVariant Identifiers: chr11:g.65635802T>G (hg19) ; chr11:g.65868331T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868331T>G , CM000673.2:g.65868331T>G	GRCh38
NC_000011.9:g.65635802T>G , CM000673.1:g.65635802T>G	GRCh37
NC_000011.8:g.65392378T>G	NCBI36
NG_012304.2:g.9604A>C
NG_053116.1:g.13270T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.938A>C MANE Select	ENSP00000309953.6:p.Asn313Thr
ENST00000307998.10:c.938A>C	ENSP00000309953.6:p.Asn313Thr
ENST00000525392.1:n.99A>C
ENST00000526628.5:n.1504A>C
ENST00000528176.5:c.938A>C	ENSP00000434151.1:p.Asn313Thr
ENST00000528409.1:n.182A>C
ENST00000530806.5:c.-61A>C	ENSP00000436526.1:n.-61A>C
ENST00000531005.5:n.1932A>C
ENST00000531645.5:c.86A>C	ENSP00000436521.1:p.Asn29Thr
ENST00000531972.5:c.938A>C	ENSP00000435295.1:p.Asn313Thr
ENST00000532084.5:n.364A>C
NM_016938.4:c.938A>C	NP_058634.4:p.Asn313Thr
NR_037718.1:n.1197A>C
NM_016938.5:c.938A>C MANE Select	NP_058634.4:p.Asn313Thr
NR_037718.2:n.1063A>C