Canonical Allele Identifier: CA12862845
Gene: LYN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.55880680A>G , CM000670.2:g.55880680A>G GRCh38
NC_000008.10:g.56793239A>G , CM000670.1:g.56793239A>G GRCh37
NC_000008.9:g.56955793A>G NCBI36
NG_029593.1:g.5854A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000519728.6:c.-6+577A>G MANE Select ENSP00000428924.1:n.-6+577A>G
ENST00000519728.5:c.-6+577A>G ENSP00000428924.1:n.-6+577A>G
ENST00000520220.6:c.-6+577A>G ENSP00000428424.1:n.-6+577A>G
NM_001111097.2:c.-6+577A>G NP_001104567.1:n.-6+577A>G
NM_002350.3:c.-6+577A>G NP_002341.1:n.-6+577A>G
XM_011517529.1:c.642+577A>G XP_011515831.1:n.642+577A>G
XM_011517530.1:c.642+577A>G XP_011515832.1:n.642+577A>G
XR_928779.1:n.1641+577A>G
XM_011517529.3:c.642+577A>G XP_011515831.1:n.642+577A>G
XM_017013415.2:c.642+577A>G XP_016868904.1:n.642+577A>G
NM_002350.4:c.-6+577A>G MANE Select NP_002341.1:n.-6+577A>G
NM_001111097.3:c.-6+577A>G NP_001104567.1:n.-6+577A>G
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