Canonical Allele Identifier: CA480991971

Gene: LIN7A MIR618

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80935757A>T , CM000674.2:g.80935757A>T	GRCh38
NC_000012.11:g.81329536A>T , CM000674.1:g.81329536A>T	GRCh37
NC_000012.10:g.79853667A>T	NCBI36
NG_050580.1:g.7167T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000552864.6:c.82+1884T>A (LIN7A) MANE Select	ENSP00000447488.1:n.82+1884T>A
ENST00000261203.7:c.82+1884T>A (LIN7A)	ENSP00000261203.3:n.82+1884T>A
ENST00000549417.5:c.64+1884T>A (LIN7A)	ENSP00000448975.1:n.64+1884T>A
ENST00000552864.5:c.82+1884T>A (LIN7A)	ENSP00000447488.1:n.82+1884T>A
NM_004664.2:c.82+1884T>A (LIN7A)	NP_004655.1:n.82+1884T>A
NR_030349.1:n.77T>A (MIR618)
XM_011538928.1:c.82+1884T>A (LIN7A)	XP_011537230.1:n.82+1884T>A
NM_001324423.1:c.-13+1884T>A (LIN7A)	NP_001311352.1:n.-13+1884T>A
NM_004664.3:c.82+1884T>A (LIN7A)	NP_004655.1:n.82+1884T>A
NR_136887.1:n.275+1884T>A (LIN7A)
NR_136888.1:n.275+1884T>A (LIN7A)
XM_011538928.3:c.43+1884T>A (LIN7A)	XP_011537230.2:n.43+1884T>A
XM_011539062.3:c.-779A>T	XP_011537364.1:n.-779A>T
NM_001324423.2:c.-13+1884T>A (LIN7A)	NP_001311352.1:n.-13+1884T>A
NR_136887.2:n.67+1884T>A (LIN7A)
NR_136888.2:n.67+1884T>A (LIN7A)
NM_004664.4:c.82+1884T>A (LIN7A) MANE Select	NP_004655.1:n.82+1884T>A
NR_136888.3:n.294+1884T>A (LIN7A)