Canonical Allele Identifier: CA1562214
Community Standard Title: NM_145038.5(DRC1):c.1391G>A (p.Arg464His)
Gene: DRC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26444943G>A , CM000664.2:g.26444943G>A GRCh38
NC_000002.11:g.26667811G>A , CM000664.1:g.26667811G>A GRCh37
NC_000002.10:g.26521315G>A NCBI36
NG_042824.1:g.48032G>A

Transcript Alleles

HGVS Amino-acid Change
NM_145038.5:c.1391G>A MANE Select NP_659475.2:p.Arg464His
ENST00000288710.7:c.1391G>A MANE Select ENSP00000288710.2:p.Arg464His
NM_145038.3:c.1391G>A NP_659475.2:p.Arg464His
NM_145038.4:c.1391G>A NP_659475.2:p.Arg464His
ENST00000288710.6:c.1391G>A ENSP00000288710.2:p.Arg464His
ENST00000483675.1:n.992G>A
ENST00000649059.1:c.1237G>A
XM_005264637.3:c.773G>A XP_005264694.1:p.Arg258His
XM_005264638.3:c.371G>A XP_005264695.1:p.Arg124His
XM_017005271.1:c.371G>A XP_016860760.1:p.Arg124His
XM_024453218.1:c.371G>A XP_024308986.1:p.Arg124His