Canonical Allele Identifier: CA338121706
Gene: CAMTA1 HGNC NCBI

Linked Data

gnomAD v4: 1-7663427-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7663427A>G , CM000663.2:g.7663427A>G GRCh38
NC_000001.10:g.7723487A>G , CM000663.1:g.7723487A>G GRCh37
NC_000001.9:g.7646074A>G NCBI36
NG_053148.1:g.883104A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000476864.2:c.880A>G ENSP00000452319.2:p.Thr294Ala
ENST00000700414.1:c.*731A>G ENSP00000514978.1:n.*731A>G
ENST00000700415.1:c.790A>G ENSP00000514979.1:p.Thr264Ala
ENST00000700417.1:c.808A>G ENSP00000514981.1:p.Thr270Ala
ENST00000700444.1:c.*649A>G ENSP00000514992.1:n.*649A>G
ENST00000303635.12:c.880A>G MANE Select ENSP00000306522.6:p.Thr294Ala
ENST00000303635.11:c.880A>G ENSP00000306522.6:p.Thr294Ala
NM_015215.3:c.880A>G NP_056030.1:p.Thr294Ala
XM_011541083.1:c.880A>G XP_011539385.1:p.Thr294Ala
XM_011541084.1:c.880A>G XP_011539386.1:p.Thr294Ala
XM_011541085.1:c.868A>G XP_011539387.1:p.Thr290Ala
XM_011541086.1:c.880A>G XP_011539388.1:p.Thr294Ala
XM_011541087.1:c.808A>G XP_011539389.1:p.Thr270Ala
XM_011541088.1:c.790A>G XP_011539390.1:p.Thr264Ala
XM_011541089.1:c.880A>G XP_011539391.1:p.Thr294Ala
XM_011541090.1:c.880A>G XP_011539392.1:p.Thr294Ala
XM_011541091.1:c.880A>G XP_011539393.1:p.Thr294Ala
XM_011541092.1:c.880A>G XP_011539394.1:p.Thr294Ala
NM_001349608.1:c.790A>G NP_001336537.1:p.Thr264Ala
NM_001349609.1:c.880A>G NP_001336538.1:p.Thr294Ala
NM_001349610.1:c.880A>G NP_001336539.1:p.Thr294Ala
NM_001349612.1:c.790A>G NP_001336541.1:p.Thr264Ala
XM_011541083.2:c.880A>G XP_011539385.1:p.Thr294Ala
XM_011541084.2:c.880A>G XP_011539386.1:p.Thr294Ala
XM_011541086.3:c.880A>G XP_011539388.1:p.Thr294Ala
XM_011541087.2:c.808A>G XP_011539389.1:p.Thr270Ala
XM_011541088.2:c.790A>G XP_011539390.1:p.Thr264Ala
XM_011541090.3:c.880A>G XP_011539392.1:p.Thr294Ala
XM_011541091.2:c.880A>G XP_011539393.1:p.Thr294Ala
XM_011541092.3:c.880A>G XP_011539394.1:p.Thr294Ala
XM_017000774.2:c.880A>G XP_016856263.1:p.Thr294Ala
XM_017000777.1:c.880A>G XP_016856266.1:p.Thr294Ala
XM_017000778.1:c.880A>G XP_016856267.1:p.Thr294Ala
NM_015215.4:c.880A>G MANE Select NP_056030.1:p.Thr294Ala
NM_001349608.2:c.790A>G NP_001336537.1:p.Thr264Ala
NM_001349609.2:c.880A>G NP_001336538.1:p.Thr294Ala
NM_001349610.2:c.880A>G NP_001336539.1:p.Thr294Ala
NM_001349612.2:c.790A>G NP_001336541.1:p.Thr264Ala