Canonical Allele Identifier: CA1561887
Community Standard Title: NM_145038.5(DRC1):c.528C>T (p.Ser176=)
Gene: DRC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26424442C>T , CM000664.2:g.26424442C>T GRCh38
NC_000002.11:g.26647310C>T , CM000664.1:g.26647310C>T GRCh37
NC_000002.10:g.26500814C>T NCBI36
NG_042824.1:g.27531C>T

Transcript Alleles

HGVS Amino-acid Change
NM_145038.5:c.528C>T MANE Select NP_659475.2:p.Ser176=
ENST00000288710.7:c.528C>T MANE Select ENSP00000288710.2:p.Ser176=
NM_145038.3:c.528C>T NP_659475.2:p.Ser176=
NM_145038.4:c.528C>T NP_659475.2:p.Ser176=
ENST00000288710.6:c.528C>T ENSP00000288710.2:p.Ser176=
ENST00000421869.5:c.356+3042C>T ENSP00000414375.1:n.356+3042C>T
ENST00000487307.5:n.247+3042C>T
ENST00000497651.1:n.418C>T
ENST00000649059.1:c.514C>T
XM_005264637.3:c.-79+3042C>T XP_005264694.1:n.-79+3042C>T
XM_005264638.3:c.-341+3042C>T XP_005264695.1:n.-341+3042C>T
XM_017005271.1:c.-353C>T XP_016860760.1:n.-353C>T
XM_024453218.1:c.-341+3042C>T XP_024308986.1:n.-341+3042C>T