Canonical Allele Identifier: CA2762313961

Gene: BMP2K

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78865741T>A , CM000666.2:g.78865741T>A	GRCh38
NC_000004.11:g.79786895T>A , CM000666.1:g.79786895T>A	GRCh37
NC_000004.10:g.80005919T>A	NCBI36
NG_047162.1:g.94364T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.1231+21T>A MANE Select	ENSP00000424668.2:n.1231+21T>A
ENST00000335016.9:c.1231+21T>A	ENSP00000334836.5:n.1231+21T>A
ENST00000389010.7:c.*207+21T>A	ENSP00000373662.3:n.*207+21T>A
ENST00000502613.1:c.308+21T>A
ENST00000502871.5:c.1231+21T>A	ENSP00000421768.1:n.1231+21T>A
ENST00000505725.1:n.534T>A
ENST00000628286.1:c.*207+21T>A	ENSP00000487317.1:n.*207+21T>A
NM_017593.3:c.1231+21T>A	NP_060063.2:n.1231+21T>A
NM_198892.1:c.1231+21T>A	NP_942595.1:n.1231+21T>A
XM_005263117.1:c.1231+21T>A	XP_005263174.1:n.1231+21T>A
XM_011532101.1:c.991+21T>A	XP_011530403.1:n.991+21T>A
XM_011532102.1:c.1231+21T>A	XP_011530404.1:n.1231+21T>A
XM_017008381.1:c.991+21T>A	XP_016863870.1:n.991+21T>A
XM_017008382.1:c.343+21T>A	XP_016863871.1:n.343+21T>A
NM_017593.4:c.1231+21T>A	NP_060063.2:n.1231+21T>A
NM_017593.5:c.1231+21T>A	NP_060063.2:n.1231+21T>A
NM_198892.2:c.1231+21T>A MANE Select	NP_942595.1:n.1231+21T>A