Canonical Allele Identifier: CA411760788

Gene: SREBF2

Linked Data

• MyVariant Identifiers: chr22:g.42276763C>A (hg19) ; chr22:g.41880759C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41880759C>A , CM000684.2:g.41880759C>A	GRCh38
NC_000022.10:g.42276763C>A , CM000684.1:g.42276763C>A	GRCh37
NC_000022.9:g.40606709C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000710853.1:c.1715C>A	ENSP00000518526.1:p.Ala572Glu
ENST00000361204.9:c.1805C>A MANE Select	ENSP00000354476.4:p.Ala602Glu
ENST00000361204.8:c.1805C>A	ENSP00000354476.4:p.Ala602Glu
ENST00000424354.5:c.1905C>A	ENSP00000395728.1:p.Gly635=
ENST00000612482.4:c.1815C>A	ENSP00000484441.1:p.Gly605=
NM_004599.3:c.1805C>A	NP_004590.2:p.Ala602Glu
NR_103834.1:n.2097C>A
XM_006724310.1:c.1715C>A	XP_006724373.1:p.Ala572Glu
XM_011530347.1:c.1430C>A	XP_011528649.1:p.Ala477Glu
XM_006724310.3:c.1715C>A	XP_006724373.1:p.Ala572Glu
XM_011530347.2:c.1430C>A	XP_011528649.1:p.Ala477Glu
XM_017028921.2:c.1805C>A	XP_016884410.1:p.Ala602Glu
XM_017028922.2:c.1805C>A	XP_016884411.1:p.Ala602Glu
XR_001755276.2:n.1948C>A
XR_001755277.2:n.1948C>A
XR_001755278.2:n.2071C>A
NM_004599.4:c.1805C>A MANE Select	NP_004590.2:p.Ala602Glu
NR_103834.2:n.2071C>A