Canonical Allele Identifier: CA2676714286

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177403620G>C , CM000667.2:g.177403620G>C GRCh38
NC_000005.9:g.176830621G>C , CM000667.1:g.176830621G>C GRCh37
NC_000005.8:g.176763227G>C NCBI36
NG_007568.1:g.10957C>G , LRG_145:g.10957C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696192.1:c.*917-3C>G (F12) ENSP00000512476.1:n.*917-3C>G
ENST00000696193.1:c.*1638-3C>G (F12) ENSP00000512477.1:n.*1638-3C>G
ENST00000696194.1:c.*841-3C>G (F12) ENSP00000512478.1:n.*841-3C>G
ENST00000696195.1:n.4054-3C>G (F12)
ENST00000696200.1:n.1592C>G (F12)
ENST00000696201.1:c.1251-3C>G (F12) ENSP00000512482.1:n.1251-3C>G
ENST00000253496.4:c.1251-3C>G (F12) MANE Select ENSP00000253496.3:n.1251-3C>G
ENST00000253496.3:c.1251-3C>G (F12) ENSP00000253496.3:n.1251-3C>G
ENST00000502598.5:c.-45+94G>C (GRK6) ENSP00000422873.1:n.-45+94G>C
ENST00000502854.5:n.748C>G (F12)
ENST00000503736.1:n.623-3C>G (F12)
ENST00000504406.5:n.131C>G (F12)
ENST00000510358.5:n.853C>G (F12)
NM_000505.3:c.1251-3C>G , LRG_145t1:c.1251-3C>G (F12) NP_000496.2:n.1251-3C>G
XM_011534461.1:c.1251-3C>G (F12) XP_011532763.1:n.1251-3C>G
XM_011534462.1:c.915-3C>G (F12) XP_011532764.1:n.915-3C>G
XM_011534462.2:c.915-3C>G (F12) XP_011532764.1:n.915-3C>G
XM_017009773.2:c.1416+6546G>C (SLC34A1) XP_016865262.1:n.1416+6546G>C
NM_000505.4:c.1251-3C>G (F12) MANE Select NP_000496.2:n.1251-3C>G