Canonical Allele Identifier: CA381310626

Gene: EFEMP2

Linked Data

• MyVariant Identifiers: chr11:g.65638826C>A (hg19) ; chr11:g.65871355C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65871355C>A , CM000673.2:g.65871355C>A	GRCh38
NC_000011.9:g.65638826C>A , CM000673.1:g.65638826C>A	GRCh37
NC_000011.8:g.65395402C>A	NCBI36
NG_012304.2:g.6580G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000307998.11:c.169G>T MANE Select	ENSP00000309953.6:p.Glu57Ter
ENST00000307998.10:c.169G>T	ENSP00000309953.6:p.Glu57Ter
ENST00000526624.5:c.169G>T	ENSP00000435419.1:p.Glu57Ter
ENST00000527378.1:c.169G>T	ENSP00000435963.1:p.Glu57Ter
ENST00000528176.5:c.169G>T	ENSP00000434151.1:p.Glu57Ter
ENST00000530850.1:c.158G>T	ENSP00000437238.1:p.Arg53Leu
ENST00000531005.5:n.665G>T
ENST00000531972.5:c.169G>T	ENSP00000435295.1:p.Glu57Ter
ENST00000533347.5:c.215G>T	ENSP00000435823.1:p.Arg72Leu
NM_016938.4:c.169G>T	NP_058634.4:p.Glu57Ter
NR_037718.1:n.428G>T
NM_016938.5:c.169G>T MANE Select	NP_058634.4:p.Glu57Ter
NR_037718.2:n.294G>T