Canonical Allele Identifier: CA2762313966

Gene: BMP2K

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78865860A>G , CM000666.2:g.78865860A>G	GRCh38
NC_000004.11:g.79787014A>G , CM000666.1:g.79787014A>G	GRCh37
NC_000004.10:g.80006038A>G	NCBI36
NG_047162.1:g.94483A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.1231+140A>G MANE Select	ENSP00000424668.2:n.1231+140A>G
ENST00000335016.9:c.1231+140A>G	ENSP00000334836.5:n.1231+140A>G
ENST00000389010.7:c.*207+140A>G	ENSP00000373662.3:n.*207+140A>G
ENST00000502613.1:c.308+140A>G
ENST00000502871.5:c.1231+140A>G	ENSP00000421768.1:n.1231+140A>G
ENST00000628286.1:c.*207+140A>G	ENSP00000487317.1:n.*207+140A>G
NM_017593.3:c.1231+140A>G	NP_060063.2:n.1231+140A>G
NM_198892.1:c.1231+140A>G	NP_942595.1:n.1231+140A>G
XM_005263117.1:c.1231+140A>G	XP_005263174.1:n.1231+140A>G
XM_011532101.1:c.991+140A>G	XP_011530403.1:n.991+140A>G
XM_011532102.1:c.1231+140A>G	XP_011530404.1:n.1231+140A>G
XM_017008381.1:c.991+140A>G	XP_016863870.1:n.991+140A>G
XM_017008382.1:c.343+140A>G	XP_016863871.1:n.343+140A>G
NM_017593.4:c.1231+140A>G	NP_060063.2:n.1231+140A>G
NM_017593.5:c.1231+140A>G	NP_060063.2:n.1231+140A>G
NM_198892.2:c.1231+140A>G MANE Select	NP_942595.1:n.1231+140A>G