Canonical Allele Identifier: CA1458157446

Gene: LNX1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.53464700A>C , CM000666.2:g.53464700A>C	GRCh38
NC_000004.11:g.54330867A>C , CM000666.1:g.54330867A>C	GRCh37
NC_000004.10:g.54025624A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263925.8:c.1893-3107T>G MANE Select	ENSP00000263925.7:n.1893-3107T>G
ENST00000263925.7:c.1893-3107T>G	ENSP00000263925.7:n.1893-3107T>G
ENST00000306888.6:c.1605-3107T>G	ENSP00000302879.2:n.1605-3107T>G
ENST00000507166.5:c.1017+38735A>C	ENSP00000423325.1:n.1017+38735A>C
NM_001126328.2:c.1893-3107T>G	NP_001119800.1:n.1893-3107T>G
NM_032622.2:c.1605-3107T>G	NP_116011.2:n.1605-3107T>G
XM_005265785.3:c.1893-3107T>G	XP_005265842.1:n.1893-3107T>G
XM_005265786.3:c.1893-3107T>G	XP_005265843.1:n.1893-3107T>G
XM_005265785.5:c.1893-3107T>G	XP_005265842.1:n.1893-3107T>G
XM_017008776.1:c.1893-3107T>G	XP_016864265.1:n.1893-3107T>G
XM_024454261.1:c.1893-3107T>G	XP_024310029.1:n.1893-3107T>G
XM_024454262.1:c.1893-3107T>G	XP_024310030.1:n.1893-3107T>G
NM_001126328.3:c.1893-3107T>G MANE Select	NP_001119800.1:n.1893-3107T>G
NM_032622.3:c.1605-3107T>G	NP_116011.2:n.1605-3107T>G