Canonical Allele Identifier: CA2049461900

Gene: LIN7A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80898148G= , CM000674.2:g.80898148G=	GRCh38
NC_000012.11:g.81291927G= , CM000674.1:g.81291927G=	GRCh37
NC_000012.10:g.79816058G=	NCBI36
NG_050580.1:g.44776C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004664.4:c.83-8779C= MANE Select	NP_004655.1:n.83-8779C=
ENST00000552864.6:c.83-8779C= MANE Select	ENSP00000447488.1:n.83-8779C=
NM_001324423.1:c.-13+39493C=	NP_001311352.1:n.-13+39493C=
NM_001324423.2:c.-13+39493C=	NP_001311352.1:n.-13+39493C=
NM_004664.2:c.83-8779C=	NP_004655.1:n.83-8779C=
NM_004664.3:c.83-8779C=	NP_004655.1:n.83-8779C=
NR_136887.1:n.275+39493C=
NR_136887.2:n.67+39493C=
NR_136888.1:n.276-8779C=
NR_136888.2:n.68-8779C=
NR_136888.3:n.295-8779C=
ENST00000261203.7:c.83-8779C=	ENSP00000261203.3:n.83-8779C=
ENST00000549417.5:c.65-8779C=	ENSP00000448975.1:n.65-8779C=
ENST00000552864.5:c.83-8779C=	ENSP00000447488.1:n.83-8779C=
XM_011538928.1:c.83-8779C=	XP_011537230.1:n.83-8779C=
XM_011538928.3:c.44-8779C=	XP_011537230.2:n.44-8779C=