Canonical Allele Identifier: CA2573054432
Community Standard Title: NM_001070.5(TUBG1):c.480-9C>G
Gene: TUBG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42612938C>G , CM000679.2:g.42612938C>G GRCh38
NC_000017.10:g.40764956C>G , CM000679.1:g.40764956C>G GRCh37
NC_000017.9:g.38018482C>G NCBI36
NG_033886.1:g.8599C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001070.5:c.480-9C>G MANE Select NP_001061.2:n.480-9C>G
ENST00000251413.8:c.480-9C>G MANE Select ENSP00000251413.2:n.480-9C>G
NM_001070.4:c.480-9C>G NP_001061.2:n.480-9C>G
ENST00000251413.7:c.480-9C>G ENSP00000251413.2:n.480-9C>G
ENST00000588056.2:n.830-9C>G
ENST00000589688.1:c.400-9C>G ENSP00000465582.1:n.400-9C>G
ENST00000589688.2:c.400-9C>G ENSP00000465582.1:n.400-9C>G
ENST00000591509.5:c.519-9C>G ENSP00000464867.1:n.519-9C>G
ENST00000679484.1:n.1064C>G
ENST00000680617.1:n.1967-9C>G
ENST00000680672.1:n.577-9C>G
ENST00000680678.1:n.577-9C>G
ENST00000681114.1:n.1967-9C>G
ENST00000681413.1:c.480-9C>G ENSP00000505664.1:n.480-9C>G
ENST00000681490.1:n.577-9C>G
ENST00000681919.1:n.2250-9C>G
ENST00000681947.1:n.577-9C>G
XM_024450904.1:c.480-9C>G XP_024306672.1:n.480-9C>G