Canonical Allele Identifier: CA6199698

Gene: GDPD4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77271354T>C , CM000673.2:g.77271354T>C	GRCh38
NC_000011.9:g.76982399T>C , CM000673.1:g.76982399T>C	GRCh37
NC_000011.8:g.76660047T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_182833.3:c.247A>G MANE Select	NP_878253.1:p.Met83Val
ENST00000315938.5:c.247A>G MANE Select	ENSP00000320815.4:p.Met83Val
NM_182833.1:c.247A>G	NP_878253.1:p.Met83Val
NM_182833.2:c.247A>G	NP_878253.1:p.Met83Val
ENST00000315938.4:c.247A>G	ENSP00000320815.4:p.Met83Val
ENST00000376217.6:c.247A>G	ENSP00000365390.2:p.Met83Val
ENST00000532155.5:n.183A>G
XM_011544826.1:c.1A>G	XP_011543128.1:p.Met1Val
XM_011544827.1:c.1A>G	XP_011543129.1:p.Met1Val
XM_011544828.1:c.1A>G	XP_011543130.1:p.Met1Val
XM_011544829.1:c.1A>G	XP_011543131.1:p.Met1Val
XM_011544830.1:c.1A>G	XP_011543132.1:p.Met1Val
XM_011544831.1:c.1A>G	XP_011543133.1:p.Met1Val
XM_011544832.1:c.1A>G	XP_011543134.1:p.Met1Val
XM_011544833.1:c.1A>G	XP_011543135.1:p.Met1Val
XM_011544833.2:c.1A>G	XP_011543135.1:p.Met1Val
XM_011544834.1:c.325A>G	XP_011543136.1:p.Met109Val
XM_017017348.2:c.1A>G	XP_016872837.1:p.Met1Val
XM_017017349.2:c.1A>G	XP_016872838.1:p.Met1Val
XM_017017350.2:c.1A>G	XP_016872839.1:p.Met1Val
XM_017017351.2:c.1A>G	XP_016872840.1:p.Met1Val