Canonical Allele Identifier: CA10273812
Gene: TTLL12 HGNC NCBI

Linked Data

dbSNP Id: rs13058467

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.43183043T>C , CM000684.2:g.43183043T>C GRCh38
NC_000022.10:g.43579049T>C , CM000684.1:g.43579049T>C GRCh37
NC_000022.9:g.41908993T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216129.7:c.284A>G MANE Select ENSP00000216129.6:p.Asn95Ser
ENST00000216129.6:c.284A>G ENSP00000216129.6:p.Asn95Ser
NM_015140.3:c.284A>G NP_055955.1:p.Asn95Ser
XM_011530015.1:c.77A>G XP_011528317.1:p.Asn26Ser
NM_015140.4:c.284A>G MANE Select NP_055955.1:p.Asn95Ser