Canonical Allele Identifier: CA389785732

Gene: BMP4

Linked Data

• gnomAD v4: 14-53952197-A-C
• MyVariant Identifiers: chr14:g.54418915A>C (hg19) ; chr14:g.53952197A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.53952197A>C , CM000676.2:g.53952197A>C	GRCh38
NC_000014.8:g.54418915A>C , CM000676.1:g.54418915A>C	GRCh37
NC_000014.7:g.53488665A>C	NCBI36
NG_009215.1:g.9640T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245451.9:c.26T>G MANE Select	ENSP00000245451.4:p.Met9Arg
ENST00000245451.8:c.26T>G	ENSP00000245451.4:p.Met9Arg
ENST00000417573.5:c.26T>G	ENSP00000394165.1:p.Met9Arg
ENST00000558984.1:c.26T>G	ENSP00000454134.1:p.Met9Arg
ENST00000559087.5:c.26T>G	ENSP00000453485.1:p.Met9Arg
ENST00000559501.1:c.-143-21T>G	ENSP00000453365.1:n.-143-21T>G
ENST00000559642.1:c.26T>G	ENSP00000453467.1:p.Met9Arg
NM_001202.3:c.26T>G	NP_001193.2:p.Met9Arg
NM_130850.2:c.26T>G	NP_570911.2:p.Met9Arg
NM_130851.2:c.26T>G	NP_570912.2:p.Met9Arg
XM_005268015.3:c.26T>G	XP_005268072.1:p.Met9Arg
NM_001202.5:c.26T>G	NP_001193.2:p.Met9Arg
NM_001347912.1:c.188-21T>G	NP_001334841.1:n.188-21T>G
NM_001347913.1:c.-143-21T>G	NP_001334842.1:n.-143-21T>G
NM_001347914.1:c.26T>G	NP_001334843.1:p.Met9Arg
NM_001347915.1:c.-143-21T>G	NP_001334844.1:n.-143-21T>G
NM_001347916.1:c.26T>G	NP_001334845.1:p.Met9Arg
NM_001347917.1:c.-143-21T>G	NP_001334846.1:n.-143-21T>G
NM_130850.4:c.26T>G	NP_570911.2:p.Met9Arg
NM_130851.3:c.26T>G	NP_570912.2:p.Met9Arg
NM_001202.6:c.26T>G MANE Select	NP_001193.2:p.Met9Arg
NM_130850.5:c.26T>G	NP_570911.2:p.Met9Arg
NM_001347913.2:c.-143-21T>G	NP_001334842.1:n.-143-21T>G
NM_001347914.2:c.26T>G	NP_001334843.1:p.Met9Arg
NM_001347915.2:c.-143-21T>G	NP_001334844.1:n.-143-21T>G
NM_130851.4:c.26T>G	NP_570912.2:p.Met9Arg