Canonical Allele Identifier: CA15734228
Gene: LIN7A HGNC NCBI

Linked Data

dbSNP Id: rs1163662

Genomic Alleles

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

Transcript Alleles

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