Canonical Allele Identifier: CA10165681
Community Standard Title: NM_001886.3(CRYBA4):c.89C>T (p.Thr30Met)
Gene: CRYBA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26623283C>T , CM000684.2:g.26623283C>T GRCh38
NC_000022.10:g.27019247C>T , CM000684.1:g.27019247C>T GRCh37
NC_000022.9:g.25349247C>T NCBI36
NG_009825.1:g.6320C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001886.3:c.89C>T MANE Select NP_001877.1:p.Thr30Met
ENST00000354760.4:c.89C>T MANE Select ENSP00000346805.3:p.Thr30Met
NM_001886.2:c.89C>T NP_001877.1:p.Thr30Met
ENST00000354760.3:c.89C>T ENSP00000346805.3:p.Thr30Met
ENST00000466315.1:n.55+648C>T
XM_006724140.2:c.104C>T XP_006724203.1:p.Thr35Met
XM_006724140.3:c.104C>T XP_006724203.1:p.Thr35Met
XM_011529898.1:c.203C>T XP_011528200.1:p.Thr68Met
XM_017028598.1:c.122C>T XP_016884087.1:p.Thr41Met