Canonical Allele Identifier: CA11004480
Gene: DRC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26454942A>G , CM000664.2:g.26454942A>G GRCh38
NC_000002.11:g.26677810A>G , CM000664.1:g.26677810A>G GRCh37
NC_000002.10:g.26531314A>G NCBI36
NG_042824.1:g.58031A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000288710.7:c.2063+152A>G MANE Select ENSP00000288710.2:n.2063+152A>G
ENST00000649059.1:c.1909+152A>G
ENST00000288710.6:c.2063+152A>G ENSP00000288710.2:n.2063+152A>G
NM_145038.3:c.2063+152A>G NP_659475.2:n.2063+152A>G
NM_145038.4:c.2063+152A>G NP_659475.2:n.2063+152A>G
XM_005264637.3:c.1445+152A>G XP_005264694.1:n.1445+152A>G
XM_005264638.3:c.1043+152A>G XP_005264695.1:n.1043+152A>G
XM_017005271.1:c.1043+152A>G XP_016860760.1:n.1043+152A>G
XM_024453218.1:c.1043+152A>G XP_024308986.1:n.1043+152A>G
NM_145038.5:c.2063+152A>G MANE Select NP_659475.2:n.2063+152A>G