Canonical Allele Identifier: CA15116497
Gene: TMEM57 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10903129

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.25442446A>G , CM000663.2:g.25442446A>G GRCh38
NC_000001.10:g.25768937A>G , CM000663.1:g.25768937A>G GRCh37
NC_000001.9:g.25641524A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001282564.1:c.81-4316A>G VV NP_001269493.1:p.=
NM_018202.5:c.81-4316A>G VV NP_060672.2:p.=
XM_005245931.1:c.81-4316A>G XP_005245988.1:p.=
XM_011541704.1:c.-531-4316A>G XP_011540006.1:p.=
XM_005245931.2:c.81-4316A>G XP_005245988.1:p.=
XM_011541704.3:c.-531-4316A>G XP_011540006.1:p.=
NM_018202.6:c.81-4316A>G VV MANE Preferred NP_060672.2:p.=
ENST00000374343.4:c.81-4316A>G ENSP00000363463.4:p.=
ENST00000399766.7:c.81-4316A>G ENSP00000382668.3:p.=