Canonical Allele Identifier: CA357378685
Gene: BMP2K HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78865696G>C , CM000666.2:g.78865696G>C GRCh38
NC_000004.11:g.79786850G>C , CM000666.1:g.79786850G>C GRCh37
NC_000004.10:g.80005874G>C NCBI36
NG_047162.1:g.94319G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.1207G>C MANE Select ENSP00000424668.2:p.Glu403Gln
ENST00000335016.9:c.1207G>C ENSP00000334836.5:p.Glu403Gln
ENST00000389010.7:c.*183G>C ENSP00000373662.3:n.*183G>C
ENST00000502613.1:c.284G>C
ENST00000502871.5:c.1207G>C ENSP00000421768.1:p.Glu403Gln
ENST00000505725.1:n.489G>C
ENST00000628286.1:c.*183G>C ENSP00000487317.1:n.*183G>C
NM_017593.3:c.1207G>C NP_060063.2:p.Glu403Gln
NM_198892.1:c.1207G>C NP_942595.1:p.Glu403Gln
XM_005263117.1:c.1207G>C XP_005263174.1:p.Glu403Gln
XM_011532101.1:c.967G>C XP_011530403.1:p.Glu323Gln
XM_011532102.1:c.1207G>C XP_011530404.1:p.Glu403Gln
XM_017008381.1:c.967G>C XP_016863870.1:p.Glu323Gln
XM_017008382.1:c.319G>C XP_016863871.1:p.Glu107Gln
NM_017593.4:c.1207G>C NP_060063.2:p.Glu403Gln
NM_017593.5:c.1207G>C NP_060063.2:p.Glu403Gln
NM_198892.2:c.1207G>C MANE Select NP_942595.1:p.Glu403Gln