Canonical Allele Identifier: CA486658941
Gene: BMP4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.54418857A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53952139A>T , CM000676.2:g.53952139A>T GRCh38
NC_000014.8:g.54418857A>T , CM000676.1:g.54418857A>T GRCh37
NC_000014.7:g.53488607A>T NCBI36
NG_009215.1:g.9698T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000245451.9:c.84T>A MANE Select ENSP00000245451.4:p.Pro28=
ENST00000245451.8:c.84T>A ENSP00000245451.4:p.Pro28=
ENST00000417573.5:c.84T>A ENSP00000394165.1:p.Pro28=
ENST00000558961.1:c.9T>A ENSP00000453691.1:p.Pro3=
ENST00000558984.1:c.84T>A ENSP00000454134.1:p.Pro28=
ENST00000559087.5:c.84T>A ENSP00000453485.1:p.Pro28=
ENST00000559501.1:c.-106T>A ENSP00000453365.1:n.-106T>A
ENST00000559642.1:c.84T>A ENSP00000453467.1:p.Pro28=
NM_001202.3:c.84T>A NP_001193.2:p.Pro28=
NM_130850.2:c.84T>A NP_570911.2:p.Pro28=
NM_130851.2:c.84T>A NP_570912.2:p.Pro28=
XM_005268015.3:c.84T>A XP_005268072.1:p.Pro28=
NM_001202.5:c.84T>A NP_001193.2:p.Pro28=
NM_001347912.1:c.225T>A NP_001334841.1:p.Pro75=
NM_001347913.1:c.-106T>A NP_001334842.1:n.-106T>A
NM_001347914.1:c.84T>A NP_001334843.1:p.Pro28=
NM_001347915.1:c.-106T>A NP_001334844.1:n.-106T>A
NM_001347916.1:c.84T>A NP_001334845.1:p.Pro28=
NM_001347917.1:c.-106T>A NP_001334846.1:n.-106T>A
NM_130850.4:c.84T>A NP_570911.2:p.Pro28=
NM_130851.3:c.84T>A NP_570912.2:p.Pro28=
NM_001202.6:c.84T>A MANE Select NP_001193.2:p.Pro28=
NM_130850.5:c.84T>A NP_570911.2:p.Pro28=
NM_001347913.2:c.-106T>A NP_001334842.1:n.-106T>A
NM_001347914.2:c.84T>A NP_001334843.1:p.Pro28=
NM_001347915.2:c.-106T>A NP_001334844.1:n.-106T>A
NM_130851.4:c.84T>A NP_570912.2:p.Pro28=