Canonical Allele Identifier: CA963265245

Gene: BMP4

Linked Data

• gnomAD v3: 14-53952385-A-ACCCCCCCCCCCCCCCCC
• gnomAD v4: 14-53952385-A-ACCCCCCCCCCCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.53952387_53952388insCCCCCCCCCCCCCCCCC , CM000676.2:g.53952387_53952388insCCCCCCCCCCCCCCCCC	GRCh38
NC_000014.8:g.54419105_54419106insCCCCCCCCCCCCCCCCC , CM000676.1:g.54419105_54419106insCCCCCCCCCCCCCCCCC	GRCh37
NC_000014.7:g.53488855_53488856insCCCCCCCCCCCCCCCCC	NCBI36
NG_009215.1:g.9451_9452insGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245451.9:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG MANE Select	ENSP00000245451.4:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG
ENST00000245451.8:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG	ENSP00000245451.4:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG
ENST00000417573.5:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG	ENSP00000394165.1:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG
ENST00000558984.1:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG	ENSP00000454134.1:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG
ENST00000559087.5:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG	ENSP00000453485.1:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG
ENST00000559501.1:c.-143-210_-143-209insGGGGGGGGGGGGGGGGG	ENSP00000453365.1:n.-143-210_-143-209insGGGGGGGGGGGGGGGGG
ENST00000559642.1:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG	ENSP00000453467.1:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG
NM_001202.3:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG	NP_001193.2:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG
NM_130850.2:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG	NP_570911.2:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG
NM_130851.2:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG	NP_570912.2:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG
XM_005268015.3:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG	XP_005268072.1:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG
NM_001202.5:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG	NP_001193.2:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG
NM_001347912.1:c.188-210_188-209insGGGGGGGGGGGGGGGGG	NP_001334841.1:n.188-210_188-209insGGGGGGGGGGGGGGGGG
NM_001347913.1:c.-143-210_-143-209insGGGGGGGGGGGGGGGGG	NP_001334842.1:n.-143-210_-143-209insGGGGGGGGGGGGGGGGG
NM_001347914.1:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG	NP_001334843.1:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG
NM_001347915.1:c.-143-210_-143-209insGGGGGGGGGGGGGGGGG	NP_001334844.1:n.-143-210_-143-209insGGGGGGGGGGGGGGGGG
NM_001347916.1:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG	NP_001334845.1:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG
NM_001347917.1:c.-143-210_-143-209insGGGGGGGGGGGGGGGGG	NP_001334846.1:n.-143-210_-143-209insGGGGGGGGGGGGGGGGG
NM_130850.4:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG	NP_570911.2:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG
NM_130851.3:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG	NP_570912.2:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG
NM_001202.6:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG MANE Select	NP_001193.2:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG
NM_130850.5:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG	NP_570911.2:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG
NM_001347913.2:c.-143-210_-143-209insGGGGGGGGGGGGGGGGG	NP_001334842.1:n.-143-210_-143-209insGGGGGGGGGGGGGGGGG
NM_001347914.2:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG	NP_001334843.1:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG
NM_001347915.2:c.-143-210_-143-209insGGGGGGGGGGGGGGGGG	NP_001334844.1:n.-143-210_-143-209insGGGGGGGGGGGGGGGGG
NM_130851.4:c.-7-157_-7-156insGGGGGGGGGGGGGGGGG	NP_570912.2:n.-7-157_-7-156insGGGGGGGGGGGGGGGGG