Canonical Allele Identifier: CA475316911

Gene: EFEMP2

Linked Data

• MyVariant Identifiers: chr11:g.65636093A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868622A>G , CM000673.2:g.65868622A>G	GRCh38
NC_000011.9:g.65636093A>G , CM000673.1:g.65636093A>G	GRCh37
NC_000011.8:g.65392669A>G	NCBI36
NG_012304.2:g.9313T>C
NG_053116.1:g.13561A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.735T>C MANE Select	ENSP00000309953.6:p.Asp245=
ENST00000307998.10:c.735T>C	ENSP00000309953.6:p.Asp245=
ENST00000526628.5:n.1301T>C
ENST00000527969.1:n.1420T>C
ENST00000528176.5:c.735T>C	ENSP00000434151.1:p.Asp245=
ENST00000531005.5:n.1729T>C
ENST00000531972.5:c.735T>C	ENSP00000435295.1:p.Asp245=
ENST00000532084.5:n.161T>C
NM_016938.4:c.735T>C	NP_058634.4:p.Asp245=
NR_037718.1:n.994T>C
NM_016938.5:c.735T>C MANE Select	NP_058634.4:p.Asp245=
NR_037718.2:n.860T>C