Canonical Allele Identifier: CA15201937
Community Standard Title: NM_145038.5(DRC1):c.1919+337C>T
Gene: DRC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26453886C>T , CM000664.2:g.26453886C>T GRCh38
NC_000002.11:g.26676754C>T , CM000664.1:g.26676754C>T GRCh37
NC_000002.10:g.26530258C>T NCBI36
NG_042824.1:g.56975C>T

Transcript Alleles

HGVS Amino-acid Change
NM_145038.5:c.1919+337C>T MANE Select NP_659475.2:n.1919+337C>T
ENST00000288710.7:c.1919+337C>T MANE Select ENSP00000288710.2:n.1919+337C>T
NM_145038.3:c.1919+337C>T NP_659475.2:n.1919+337C>T
NM_145038.4:c.1919+337C>T NP_659475.2:n.1919+337C>T
ENST00000288710.6:c.1919+337C>T ENSP00000288710.2:n.1919+337C>T
ENST00000649059.1:c.1765+337C>T
XM_005264637.3:c.1301+337C>T XP_005264694.1:n.1301+337C>T
XM_005264638.3:c.899+337C>T XP_005264695.1:n.899+337C>T
XM_017005271.1:c.899+337C>T XP_016860760.1:n.899+337C>T
XM_024453218.1:c.899+337C>T XP_024308986.1:n.899+337C>T