Canonical Allele Identifier: CA357378732
Gene: BMP2K HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78865720G>T , CM000666.2:g.78865720G>T GRCh38
NC_000004.11:g.79786874G>T , CM000666.1:g.79786874G>T GRCh37
NC_000004.10:g.80005898G>T NCBI36
NG_047162.1:g.94343G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000502613.3:c.1231G>T MANE Select ENSP00000424668.2:p.Gly411Trp
ENST00000335016.9:c.1231G>T ENSP00000334836.5:p.Gly411Trp
ENST00000389010.7:c.*207G>T ENSP00000373662.3:n.*207G>T
ENST00000502613.1:c.308G>T
ENST00000502871.5:c.1231G>T ENSP00000421768.1:p.Gly411Trp
ENST00000505725.1:n.513G>T
ENST00000628286.1:c.*207G>T ENSP00000487317.1:n.*207G>T
NM_017593.3:c.1231G>T NP_060063.2:p.Gly411Trp
NM_198892.1:c.1231G>T NP_942595.1:p.Gly411Trp
XM_005263117.1:c.1231G>T XP_005263174.1:p.Gly411Trp
XM_011532101.1:c.991G>T XP_011530403.1:p.Gly331Trp
XM_011532102.1:c.1231G>T XP_011530404.1:p.Gly411Trp
XM_017008381.1:c.991G>T XP_016863870.1:p.Gly331Trp
XM_017008382.1:c.343G>T XP_016863871.1:p.Gly115Trp
NM_017593.4:c.1231G>T NP_060063.2:p.Gly411Trp
NM_017593.5:c.1231G>T NP_060063.2:p.Gly411Trp
NM_198892.2:c.1231G>T MANE Select NP_942595.1:p.Gly411Trp